EP1040118A1 - Secreted proteins and polynucleotides encoding them - Google Patents
Secreted proteins and polynucleotides encoding themInfo
- Publication number
- EP1040118A1 EP1040118A1 EP98959599A EP98959599A EP1040118A1 EP 1040118 A1 EP1040118 A1 EP 1040118A1 EP 98959599 A EP98959599 A EP 98959599A EP 98959599 A EP98959599 A EP 98959599A EP 1040118 A1 EP1040118 A1 EP 1040118A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- seq
- nucleotide
- polynucleotide
- sequence
- nucleotide sequence
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- the present invention provides novel polynucleotides and proteins encoded by such polynucleotides, along with therapeutic, diagnostic and research utilities for these polynucleotides and proteins.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment comprising eight consecutive amino acids of SEQ ID NO:2;
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO:l from nucleotide 63 to nucleotide 1265; the nucleotide sequence of SEQ ID NO:l from nucleotide 132 to nucleotide 1265; the nucleotide sequence of the full-length protein coding sequence of clone bd306_7 deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone bd306_7 deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone bd306_7 deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:2 from amino acid 148 to amino acid 189.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:2, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment comprising the amino acid sequence from amino acid 195 to amino acid 204 of SEQ ID NO:2.
- inventions provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of:
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:l, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:l to a nucleotide sequence corresponding to the 3' end of SEQ ID NO:l , but excluding the poly(A) tail at the 3' end of SEQ ID NO:l.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:l from nucleotide 63 to nucleotide 1265, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:l from nucleotide 63 to nucleotide 1265, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NOJ from nucleotide 63 to nucleotide 1265.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NOJ from nucleotide 132 to nucleotide 1265, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:l from nucleotide 132 to nucleotide 1265, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:l from nucleotide 132 to nucleotide 1265.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- protein comprises the amino acid sequence of SEQ ID NO:2 or the amino acid sequence of SEQ ID NO:2 from amino acid 148 to amino acid 189.
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:2, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment comprising the amino acid sequence from amino acid 195 to amino acid 204 of SEQ ID NO:2.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- a polynucleotide wtiich encodes a species homologue of the protein of (h) or (i) above ;
- polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i).
- polynucleotide comprises the nucleotide sequence of SEQ ID NO: 1
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone fj283_ll deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:4 from amino acid 1 to amino acid 27.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:4, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment comprising the amino acid sequence from amino acid 184 to amino acid 193 of SEQ ID NO:4.
- step (ba) SEQ ID NO:3, but excluding the poly(A) tail at the 3' end of SEQ ID NO:3; and (bb) the nucleotide sequence of the cDNA insert of clone fj283_ll deposited under accession number ATCC 98599; and (ii) hybridizing said primer(s) to human DNA; (iii) amplifying human DNA sequences; and (iv) isolating the polynucleotide product of step (b)(iii).
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:3, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:3 to a nucleotide sequence corresponding to the 3' end of SEQ ID NO:3 , but excluding the poly(A) tail at the 3' end of SEQ ID NO:3.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:3 from nucleotide 719 to nucleotide 1855, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:3 from nucleotide 719 to nucleotide 1855, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:3 from nucleotide 719 to nucleotide 1855.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:3 from nucleotide 779 to nucleotide 1855, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:3 from nucleotide 779 to nucleotide 1855, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:3 from nucleotide 779 to nucleotide 1855.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- protein comprises the amino acid sequence of SEQ ID NO:4 or the amino acid sequence of SEQ ID NO:4 from amino acid 1 to amino acid 27.
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:4, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment comprising the amino acid sequence from amino acid 184 to amino acid 193 of SEQ ID NO:4.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID
- polynucleotide which encodes a species homologue of the protein of (i) or (j) above ; and (m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(j).
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO:32 from nucleotide 982 to nucleotide 2118; the nucleotide sequence of SEQ ID NO:32 from nucleotide 1042 to nucleotide 2118; the nucleotide sequence of SEQ ID NO:32 from nucleotide 621 to nucleotide 1248; the nucleotide sequence of the full-length protein coding sequence of clone fj283_6 deposited under accession number ATCC xxxxx; or the nucleotide sequence of a mature protein coding sequence of clone fj283_6 deposited under accession number ATCC xxxxx.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone fj283_6 deposited under accession number ATCC xxxxx.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:4, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment comprising the amino acid sequence from amino acid 184 to amino acid 193 of SEQ ID NO:4.
- inventions provide the gene corresponding to the cDNA sequence of SEQ ID NO:32.
- Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of:
- step (ii) hybridizing said primer(s) to human DNA; (iii) amplifying human DNA sequences; and (iv) isolating the polynucleotide product of step (b)(iii).
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:32, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:32 to a nucleotide sequence corresponding to the 3' end of SEQ ID NO:32 , but excluding the poly(A) tail at the 3' end of SEQ ID NO:32.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:32 from nucleotide 982 to nucleotide 2118, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:32 from nucleotide 982 to nucleotide 2118, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:32 from nucleotide 982 to nucleotide 2118.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:32 from nucleotide 1042 to nucleotide 2118, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:32 from nucleotide 1042 to nucleotide 2118, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:32 from nucleotide 1042 to nucleotide 2118.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:32 from nucleotide 621 to nucleotide 1248, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:32 from nucleotide 621 to nucleotide 1248, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:32 from nucleotide 621 to nucleotide 1248.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment comprising eight consecutive amino acids of SEQ ID NO:6;
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO:5 from nucleotide 259 to nucleotide 624; the nucleotide sequence of the full-length protein coding sequence of clone fk317_3 deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone fk317_3 deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone fk317_3 deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:6 from amino acid 1 to amino acid 72.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:6, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment comprising the amino acid sequence from amino acid 56 to amino acid 65 of SEQ ID NO:6.
- inventions provide the gene corresponding to the cDNA sequence of SEQ ID NO:5.
- Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of:
- step (iii) amplifying human DNA sequences; and (iv) isolating the polynucleotide product of step (b)(iii).
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:5, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:5 to a nucleotide sequence corresponding to the 3' end of SEQ ID NO:5 , but excluding the poly(A) tail at the 3' end of SEQ ID NO:5.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:5 from nucleotide 259 to nucleotide 624, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:5 from nucleotide 259 to nucleotide 624, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:5 from nucleotide 259 to nucleotide 624.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of: (a) the amino acid sequence of SEQ ID NO:6;
- amino acid sequence of SEQ ID NO:6 comprising eight consecutive amino acids of SEQ ID NO:6; and (d) the amino acid sequence encoded by the cDNA insert of clone fk317_3 deposited under accession number ATCC 98599; the protein being substantially free from other mammalian proteins.
- protein comprises the amino acid sequence of SEQ ID NO:6 or the amino acid sequence of SEQ ID NO:6 from amino acid 1 to amino acid 72.
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:6, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment comprising the amino acid sequence from amino acid 56 to amino acid 65 of SEQ ID NO:6.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment comprising eight consecutive amino acids of SEQ ID NO:8;
- (k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above ; and (1) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i).
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO: 1
- polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone k213_2x deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:8, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment comprising the amino acid sequence from amino acid 32 to amino acid 41 of SEQ ID NO:8.
- step (ba) SEQ ID NO:7, but excluding the poly(A) tail at the 3' end of SEQ ID NO:7; and (bb) the nucleotide sequence of the cDNA insert of clone l 213_2x deposited under accession number ATCC 98599; and (ii) hybridizing said primer(s) to human DNA; (iii) amplifying human DNA sequences; and (iv) isolating the polynucleotide product of step (b)(iii).
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:7, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:7 to a nucleotide sequence corresponding to the 3' end of SEQ ID NO:7 , but excluding the poly(A) tail at the 3' end of SEQ ID NO:7.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:7 from nucleotide 357 to nucleotide 578, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:7 from nucleotide 357 to nucleotide 578, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:7 from nucleotide 357 to nucleotide 578.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:7 from nucleotide 471 to nucleotide 578, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:7 from nucleotide 471 to nucleotide 578, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:7 from nucleotide 471 to nucleotide 578.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:8, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment comprising the amino acid sequence from amino acid 32 to amino acid 41 of SEQ ID NO:8.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: (a) a polynucleotide comprising the nucleotide sequence of SEQ ID
- polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i).
- polynucleotide comprises the nucleotide sequence of SEQ ID NO: 1
- polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone na316_l deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NOJO having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NOJO, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NOJO having biological activity, the fragment comprising the amino acid sequence from amino acid 39 to amino acid 48 of SEQ ID NOJO.
- Other embodiments provide the gene corresponding to the cDNA sequence of SEQ
- inventions provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of: (i) preparing one or more polynucleotide probes that hybridize in 6X SSC at 65 degrees C to a nucleotide sequence selected from the group consisting of:
- the polynucleotide isolated accordmg to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO.9, and extendmg contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:9 to a nucleotide sequence correspondmg to the 3' end of SEQ ID NO.9 , but excluding the poly(A) tail at the 3' end of SEQ ID NO.9
- the polynucleotide isolated accordmg to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:9 from nucleotide 332 to nucleotide 598, and extendmg contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of
- SEQ ID NO:9 from nucleotide 332 to nucleotide 598, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:9 from nucleotide 332 to nucleotide 598.
- the polynucleotide isolated accordmg to the above process comprises a nucleotide sequence correspondmg to the cDNA sequence of SEQ ID NO:9 from nucleotide 458 to nucleotide 598, and extendmg contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:9 from nucleotide 458 to nucleotide 598, to a nucleotide sequence correspondmg to the 3' end of said sequence of SEQ ID NO:9 from nucleotide 458 to nucleotide 598
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NOJO having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NOJO, or a protein comprising a fragment of the amino acid sequence of SEQ ID NOJO having biological activity, the fragment comprising the amino acid sequence from amino acid 39 to amino acid 48 of SEQ ID NOJO.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- (k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above ; and (1) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i).
- such polynucleotide comprises the nucleotide sequence of SEQ ID NOJ1 from nucleotide 354 to nucleotide 986; the nucleotide sequence of SEQ ID NO:ll from nucleotide 408 to nucleotide 986; the nucleotide sequence of the full-length protein coding sequence of clone nf93_20 deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone nf93_20 deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone nf93_20 deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO: 12 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:12, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment comprising the amino acid sequence from amino acid 100 to amino acid 109 of SEQ ID NO:12.
- step (ba) SEQ ID NO:ll, but excluding the poly(A) tail at the 3' end of SEQ ID NOJ1; and (bb) the nucleotide sequence of the cDNA insert of clone nf93_20 deposited under accession number ATCC 98599; and (ii) hybridizing said primer(s) to human DNA; (iii) amplifying human DNA sequences; and (iv) isolating the polynucleotide product of step (b)(iii).
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:ll, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NOJ1 to a nucleotide sequence corresponding to the 3' end of SEQ ID NO:ll , but excluding the poly(A) tail at the 3' end of SEQ ID NO:ll.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO: 11 from nucleotide 354 to nucleotide 986, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:ll from nucleotide 354 to nucleotide 986, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO: 11 from nucleotide 354 to nucleotide 986.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO: 11 from nucleotide 408 to nucleotide 986, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO: 11 from nucleotide 408 to nucleotide 986, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NOJ1 from nucleotide 408 to nucleotide 986.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:12, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO: 12 having biological activity, the fragment comprising the amino acid sequence from amino acid 100 to amino acid 109 of SEQ ID NO:12.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO:13 from nucleotide 301 to nucleotide 1821; the nucleotide sequence of SEQ ID NO:13 from nucleotide 1381 to nucleotide 1821; the nucleotide sequence of the full-length protein coding sequence of clone npl64_l deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone npl64_l deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone npl64_l deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NOJ4 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:14, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment comprising the amino acid sequence from amino acid 248 to amino acid 257 of SEQ ID NO: 14.
- inventions provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of: (i) preparing one or more polynucleotide probes that hybridize in 6X SSC at 65 degrees C to a nucleotide sequence selected from the group consisting of:
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:13, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:13 from nucleotide 301 to nucleotide 1821, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:13 from nucleotide 301 to nucleotide 1821, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:13 from nucleotide 301 to nucleotide 1821.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NOJ3 from nucleotide 1381 to nucleotide 1821, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:13 from nucleotide 1381 to nucleotide 1821, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NOJ3 from nucleotide 1381 to nucleotide 1821.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO: 14, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment comprising the amino acid sequence from amino acid 248 to amino acid 257 of SEQ ID NO:14.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO:15 from nucleotide 148 to nucleotide 537; the nucleotide sequence of the full-length protein coding sequence of clone pe204_l deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone pe204_l deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone pe204_l deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO: 16 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:16, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment comprising the amino acid sequence from amino acid 60 to amino acid 69 of SEQ ID NO:16.
- inventions provide the gene corresponding to the cDNA sequence of SEQ ID NO:15.
- Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of: (i) preparing one or more polynucleotide probes that hybridize in 6X SSC at 65 degrees C to a nucleotide sequence selected from the group consisting of:
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:15, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:15 from nucleotide 148 to nucleotide 537, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:15 from nucleotide 148 to nucleotide 537, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO: 15 from nucleotide 148 to nucleotide 537.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:16, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment comprising the amino acid sequence from amino acid 60 to amino acid 69 of SEQ ID NO:16.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- (k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above ; and (1) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i).
- such polynucleotide comprises the nucleotide sequence of SEQ ID NOJ7 from nucleotide 24 to nucleotide 1109; the nucleotide sequence of SEQ ID NO:17 from nucleotide 1050 to nucleotide 1109; the nucleotide sequence of the fuU-length protein coding sequence of clone yal_l deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone yal_l deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yal_l deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO: 18 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:18, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO: 18 having biological activity, the fragment comprising the amino acid sequence from amino acid 176 to amino acid 185 of SEQ ID NO:18.
- step (ba) SEQ ID NO:17, but excluding the poly(A) tail at the 3' end of SEQ ID NOJ7; and (bb) the nucleotide sequence of the cDNA insert of clone yal_l deposited under accession number ATCC 98599; and (ii) hybridizing said primer(s) to human DNA; (iii) amplifying human DNA sequences; and (iv) isolating the polynucleotide product of step (b)(iii).
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:17, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ ID NO:17 to a nucleotide sequence corresponding to the 3' end of SEQ ID NOJ7 , but excluding the poly(A) tail at the 3' end of SEQ ID NO:17.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO: 17 from nucleotide 24 to nucleotide 1109, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:17 from nucleotide 24 to nucleotide 1109, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NOJ7 from nucleotide 24 to nucleotide 1109.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:17 from nucleotide 1050 to nucleotide 1109, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:17 from nucleotide 1050 to nucleotide 1109, to a nucleotide sequence correspondmg to the 3' end of said sequence of SEQ ID NO:17 from nucleotide 1050 to nucleotide 1109.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:18, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment comprising the amino acid sequence from amino acid 176 to amino acid 185 of SEQ ID NO:18.
- the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:
- polynucleotide which encodes a species homologue of the protein of (i) or (j) above ; and (m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(j).
- such polynucleotide comprises the nucleotide sequence of SEQ ID NO:19 from nucleotide 27 to nucleotide 734; the nucleotide sequence of SEQ ID NO:19 from nucleotide 270 to nucleotide 734; the nucleotide sequence of SEQ ID NO:19 from nucleotide 85 to nucleotide 1604; the nucleotide sequence of the full-length protein coding sequence of clone yb8_l deposited under accession number ATCC 98599; or the nucleotide sequence of a mature protein coding sequence of clone yb8_l deposited under accession number ATCC 98599.
- the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb8_l deposited under accession number ATCC 98599.
- the present invention provides a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:20 from amino acid 70 to amino acid 236.
- the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:20, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment comprising the amino acid sequence from amino acid 113 to amino acid 122 of SEQ ID NO:20.
- Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:19.
- inventions provide isolated polynucleotides produced according to a process selected from the group consisting of: (a) a process comprising the steps of:
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO: 19, and extending contiguously from a nucleotide sequence corresponding to the 5' end of SEQ
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:19 from nucleotide 27 to nucleotide 734, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO: 19 from nucleotide 27 to nucleotide 734, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO: 19 from nucleotide 27 to nucleotide 734.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:19 from nucleotide 270 to nucleotide 734, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:19 from nucleotide 270 to nucleotide 734, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:19 from nucleotide 270 to nucleotide 734.
- the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:19 from nucleotide 85 to nucleotide 1604, and extending contiguously from a nucleotide sequence corresponding to the 5' end of said sequence of SEQ ID NO:19 from nucleotide 85 to nucleotide 1604, to a nucleotide sequence corresponding to the 3' end of said sequence of SEQ ID NO:19 from nucleotide 85 to nucleotide 1604.
- the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:
- protein comprises the amino acid sequence of SEQ ID NO:20 or the amino acid sequence of SEQ ID NO:20 from amino acid 70 to amino acid 236.
- the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) consecutive amino acids of SEQ ID NO:20, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment comprising the amino acid sequence from amino acid 113 to amino acid 122 of SEQ ID NO:20.
- the polynucleotide is operably linked to an expression control sequence.
- the invention also provides a host cell, including bacterial, yeast, insect and mammalian cells, transformed with such polynucleotide compositions. Also provided by the present invention are organisms that have enhanced, reduced, or modified expression of the gene(s) corresponding to the polynucleotide sequences disclosed herein.
- Processes are also provided for producing a protein, which comprise:
- the protein produced according to such methods is also provided by the present invention.
- Protein compositions of the present invention may further comprise a pharmaceutically acceptable carrier.
- Compositions comprising an antibody which specifically reacts with such protein are also provided by the present invention.
- Methods are also provided for preventing, treating or ameliorating a medical condition which comprises administering to a mammalian subject a therapeutically effective amount of a composition comprising a protein of the present invention and a pharmaceutically acceptable carrier.
- Figures 1 A and IB are schematic representations of the pED6 and pNOTs vectors, respectively, used for deposit of clones disclosed herein.
- nucleotide and amino acid sequences are reported below for each clone and protein disclosed in the present application.
- the nucleotide sequence of each clone can readily be determined by sequencing of the deposited clone in accordance with known methods. The predicted amino acid sequence (both full-length and mature forms) can then be determined from such nucleotide sequence.
- the amino acid sequence of the protein encoded by a particular clone can also be determined by expression of the clone in a suitable host cell, collecting the protein and determining its sequence. For each disclosed protein applicants have identified what they have determined to be the reading frame best identifiable with sequence information available at the time of filing.
- a "secreted” protein is one which, when expressed in a suitable host cell, is transported across or through a membrane, including transport as a result of signal sequences in its amino acid sequence.
- "Secreted” proteins include without limitation proteins secreted wholly (e.g., soluble proteins) or partially (e.g. , receptors) from the cell in which they are expressed.
- “Secreted” proteins also include without limitation proteins which are transported across the membrane of the endoplasmic reticulum.
- a polynucleotide of the present invention has been identified as clone "bd306_7".
- bd306_7 was isolated from a hum-an fetal kidney cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- bd306_7 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as "bd306_7 protein").
- nucleotide sequence of bd306_7 as presently determined is reported in SEQ ID NO:l, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the bd306_7 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:2.
- Amino acids 11 to 23 are a predicted leader /signal sequence, with the predicted mature amino acid sequence beginning at amino acid 24. Due to the hydrophobic nature of the predicted leader /signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the bd306_7 protein.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone bd306_7 should be approximately 3700 bp.
- bd306_7 demonstrated at least some similarity with sequences identified as AA027096 (zk04d03.sl Soares pregnant uterus NbHPU Homo sapiens cDNA clone 469541 3'), AA027135 (zk04d03.rl Soares pregnant uterus NbHPU Homo sapiens cDNA clone 469541 5'), AA166312 (ms42gll.rl Life Tech mouse embryo 135dpc 10666014 Mus musculus cDNA clone 6142765' similar to TR E238793 E238793 DUALIN), AA535890 (nf94a03.sl NCI_CGAP_Co3 Homo sapiens cDNA clone IMAGE:927532), H144
- the predicted amino acid sequence disclosed herein for bd306_7 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol.
- the predicted bd306_7 protein demonstrated at least some similarity to sequences identified as R95913 (Neural thread protein [Homo sapiens]), U47621 (nucleolar autoantigen No55 [Homo sapiens]), and X97607 (cartilage associated protein [Gallus gallus]).
- Two regions of bd306_7 protein align with the same region, amino acids 145-214, of cartilage associated protein.
- bd306_7 proteins and each similar protein or peptide may share at least some activity.
- the nucleotide sequence of bd306_7 also indicates that it may contain an Alu repetitive element.
- fj283_ll and fj283_6 Polynucleotides of the present invention have been identified as clone "fj283_ll” and clone “fj283_6”.
- fj283_ll and fj283_6 were isolated from a human adult lung carcinoma cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or were identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- fj283_ll and fj283_6 are full-length clones, including the entire coding sequence of a secreted protein (also referred to herein as "fj283 protein").
- nucleotide sequence of fj283_6 as presently determined is reported in SEQ ID NO:32, and includes a poly(A) tail.
- cDNA clones .fj283_ll and fj283_6 have different nucleotide sequences, perhaps as a result of alternative splicing of a common primary mRNA transcript (particularly between nucleotide 402 and nucleotide 618 of SEQ ID NO:32), these clones are predicted to encode the same protein. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the fj283 protein corresponding to the foregoing nucleotide sequences is reported in SEQ ID NO:4.
- Amino acids 8 to 20 of SEQ ID NO:4 are a predicted leader /signal sequence, with the predicted mature amino acid sequence beginning at amino acid 21. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader /signal sequence not be separated from the remainder of the fj283 protein.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone fj283_ll should be approximately 3350 bp.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone fj283_6 should be approximately 2700 bp.
- the nucleotide sequences disclosed herein for fj283_ll and fj283_6 were searched against the GenBank and GeneSeq nucleotide sequence databases using
- fj283_ll and/or fj283_6 demonstrated at least some similarity with sequences identified as AA052962 (zl70c02.sl Sfratagene colon (#937204) Homo sapiens cDNA clone 509954 3' similar to gb D14531 60S RIBOSOMAL PROTEIN L9 (HUMAN)), AA080949 (zn04dl2.rl Sfratagene hNT), AAl 60948 (zq40el2.rl Sfratagene hNT neuron (#937233) Homo sapiens cDNA clone 6322065'), AA195089 (zr34c02.rl Soares NhHMPu SI Homo sapiens cDNA clone 665282 5', mRNA sequence), AA258887 (zs32b02.rl NCI_CGAP_GCB1 Homo sapiens
- the predicted amino acid sequence disclosed herein for the fj283 protein was searched against the Ge.rtPept and GeneSeq amino acid sequence databases using the BLASTX search protocol.
- the predicted fj283 protein demonstrated at least some similarity to sequences identified as AB011084 (KIAA0512 protein [Homo sapiens]) and U09953 (ribosomal protein L9 [Homo sapiens]). Based upon sequence similarity, fj283 proteins and each similar protein or peptide may share at least some activity.
- Profile hidden markov model analysis has revealed the presence of an Armadillo /beta-catenin-like domain within the predicted fj283 protein sequence.
- the armadillo multigene family comprises many proteins widely differing in sizes and functions which have in common a variable number of tandemly repeated arm sequences of about 42 amino acids in length. Many, but not all, armadillo-repeat- containing proteins are nuclear in localization. The predicted fj283 protein does not appear to be of the nuclear variety, but rather appears to be an extracellular protein.
- fk317_3 A polynucleotide of the present invention has been identified as clone "fk317_3".
- fk317_3 was isolated from a human adult kidney cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- fk317_3 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as "fk317_3 protein").
- nucleotide sequence of fk317_3 as presently determined is reported in SEQ ID NO:5, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the fk317_3 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:6.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone fk317_3 should be approximately 1400 bp.
- fk317_3 The nucleotide sequence disclosed herein for fk317_3 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. fk317_3 demonstrated at least some similarity with sequences identified as AA568588 (nm21bll.sl NCI_CGAP_ColO Homo sapiens cDNA clone IMAGEJ060797), AC002326 (Genomic sequence from Human 6, complete sequence), H48562 (yq78g07.sl Homo sapiens cDNA clone 201948 3' similar to contains Alu repetitive element; contains MER30 repetitive element), T67164 (Human alpha-N- acetylglucosaminidase gene), and Z46941 (H.sapiens DNA for alu repeats).
- the predicted amino acid sequence disclosed herein for fk317_3 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol.
- the predicted fl 317_3 protein demonstrated at least some similarity to sequences identified as X55777 (put. ORF [Homo sapiens]). Based upon sequence similarity, fk317_3 proteins and each similar protein or peptide may share at least some activity.
- the TopPredll computer program predicts a potential tr,ansmembrane domain within the fk317_3 protein sequence centered around amino acid 42 of SEQ ID NO:6.
- the nucleotide sequence of fk317_3 indicates that it may contain an Alu repetitive element.
- a polynucleotide of the present invention has been identified as clone "k213_2x".
- Secreted cDNA clones were first isolated from a murine adult bone marrow (stromal cell line FCM-4) cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or were identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- k213_2x a full- length human cDNA clone, including the entire coding sequence of a secreted protein (also referred to herein as "lc213_2x protein").
- the nucleotide sequence of k213_2x as presently determined is reported in SEQ ID NO: 1
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone k213_2x should be approximately 1900 bp.
- the nucleotide sequence disclosed herein for k213_2x was searched against the
- k213_2x demonstrated at least some similarity with sequences identified as AA123852 (mp96e08.rl Soares 2NbMT Mus musculus cDNA clone 577094 5'), AA362005 (EST71348 T-cell lymphoma Homo sapiens cDNA 5' end), AA436477 (zv08f05.sl Soares NhHMPu SI Homo sapiens cDNA clone 753057 3"), AA436528 (zv08f05.rl Soares NhHMPu SI Homo sapiens cDNA clone 753057 5"), AA643506 (nq86f04.sl NCI_CGAP_Co9 Homo sapiens cDNA clone IMAGEJ159231, mRNA sequence), F13485 (H.
- k213_2x proteins and each similar protein or peptide may share at least some activity.
- na316_l A polynucleotide of the present invention has been identified as clone "na316_l”.
- na316_l was isolated from a human adult brain (corpus callosum) cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- na316_l is a full- length clone, including the entire coding sequence of a secreted protein (also referred to herein as "na316_l protein").
- nucleotide sequence of na316_l as presently determined is reported in SEQ ID NO:9, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the na316_l protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NOJO.
- Amino acids 30 to 42 are a predicted leader /signal sequence, with the predicted mature amino acid sequence beginning at amino acid 43. Due to the hydrophobic nature of the predicted leader /signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the na316_l protein.
- T e EcoRI/NotI restriction fragment obtainable from the deposit containing clone na316_l should be approximately 900 bp.
- na316_l The nucleotide sequence disclosed herein for na316_l was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No hits were found in the database.
- the TopPredll computer program predicts two potential transmembrane domains within the na316_l protein sequence, centered around amino acids 31 and 66 of SEQ ID NOJO, respectively.
- nf93_20 A polynucleotide of the present invention has been identified as clone "nf93_20".
- nf93_20 was isolated from a human adult brain (substantia nigra) cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- nf93_20 is a full- length clone, including the entire coding sequence of a secreted protein (also referred to herein as "nf93_20 protein").
- nucleotide sequence of nf93_20 as presently determined is reported in SEQ ID NOJ1, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ni93_20 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:12. Amino acids 6 to 18 are a predicted leader/ signal sequence, with the predicted mature amino acid sequence beginning at amino acid 19. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader /signal sequence not be separated from the remainder of the nf93_20 protein.
- the EcoRI /NotI restriction fragment obtainable from the deposit containing clone nf93_20 should be approximately 2000 bp.
- nf93_20 The nucleotide sequence disclosed herein for nf93_20 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols, nf 93_20 demonstrated at least some similarity with sequences identified as AA063620 (ze87g07.sl Soares fetal heart NbHH19W Homo sapiens cDNA clone 366012 3"), AA317410 (EST19337 Retina II Homo sapiens cDNA 5' end), H29417
- nf93_20 proteins and each similar protein or peptide may share at least some activity.
- npl64_l A polynucleotide of the present invention has been identified as clone "npl64_l”.
- npl64_l was isolated from a human fetal kidney (293 cell line) cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- npl64_l is a full- length clone, including the entire coding sequence of a secreted protein (also referred to herein as "npl64_l protein").
- nucleotide sequence of npl64_l as presently determined is reported in SEQ ID NO:13, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the npl64_l protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:14.
- Amino acids 348 to 360 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 361. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the npl64_l protein.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone npl64_l should be approximately 2100 bp.
- the nucleotide sequence disclosed herein for npl64_l was searched against the
- npl64_l demonstrated at least some similarity with sequences identified as N63143 (yz37cl2.sl Homo sapiens cDNA clone 285238 3'), T19992 (Human gene signature HUMGS01129), Z46676 (Caenorhabditis elega s cosmid C08B11, complete sequence), and Z74910 (S.cerevisiae chromosome XV reading frame ORF YOR002w).
- npl64_l The predicted amino acid sequence disclosed herein for npl64_l was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol.
- the predicted npl64_l protein demonstrated at least some similarity to sequences identified as Z46676 (C08B11.8 [Caenorhabditis elegans]) and Z74910 (ORF YOR002w [Saccharomyces cerevisiae]). Based upon sequence similarity, npl64_l proteins and each similar protein or peptide may share at least some activity.
- the TopPredll computer program predicts ten potential transmembrane domains within the npl64_l protein sequence, centered around amino acids 4, 114, 165, 229, 293, 322, 360, 386, 436, and 465 of SEQ ID NO:14, respectively.
- pe204_l A polynucleotide of the present invention has been identified as clone "pe204_l".
- pe204_l was isolated from a human adult blood (chronic myelogenous leukemia K5) cDNA library using methods which are selective for cDNAs encoding secreted proteins (see U.S. Pat. No. 5,536,637), or was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- pe204_l is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as "pe204_l protein").
- the nucleotide sequence of pe204_l as presently determined is reported in SEQ ID NO:15, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the pe204_l protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:16.
- Amino acids 116 to 128 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 129. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the pe204_l protein.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone pe204_l should be approximately 1100 bp.
- pe204_l demonstrated at least some similarity with sequences identified as AA279961 (zs92h08.sl NCI_CGAP_GCB1 Homo sapiens cDNA clone 704991 3'), AA306911 (EST178043 Colon carcinoma (HCC) ceU line Homo sapiens cDNA 5' end), AC002086 (Human PAC clone DJ525N14), AC002094 (Genomic sequence from Human 17, complete sequence), T97749 (ye58c04.sl Homo sapiens cDNA clone), Z74696 (Human DNA sequence from cosmid 203C2, between markers DXS6791 and DXS8038 on chromosome X contains ESTs), Z80901 (Human DNA sequence from cosmid N119A7 on
- the predicted amino acid sequence disclosed herein for pe204_l was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol.
- the predicted pe204_l protein demonstrated at least some similarity to sequences identified as K02113 (Gallus gallus vitellogenin [Gallus gallus]). Based upon sequence similarity, pe204_l proteins and each similar protein or peptide may share at least some activity.
- the TopPredll computer program predicts two additional potential transmembrane domains within the pe204_l protein sequence, one centered around amino acid 50 and another around amino acid 90 of SEQ ID NO:16.
- yal_l A polynucleotide of the present invention has been identified as clone "yal_l".
- yal_l was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- yal_l is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as "yal_l protein").
- nucleotide sequence of yal_l as presently determined is reported in SEQ ID NO:17, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yal_l protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NOJ8. Amino acids 330 to
- 342 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 343. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader /signal sequence not be separated from the remainder of the yal_l protein.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone yal_l should be approximately 1400 bp.
- yal_l demonstrated at least some similarity with sequences identified as AA431507 (zw76e05.rl Soares testis NHT Homo sapiens cDNA clone 782144 5') and F03332 (H. sapiens partial cDNA sequence; clone c-ltg07). Based upon sequence similarity, yal_l proteins and each similar protein or peptide may share at least some activity.
- the TopPredll computer program predicts two potential transmembrane domains within the yal_l protein sequence centered around amino acid 156 and around amino acid 332 of SEQ ID NO:18, respectively.
- the nucleotide sequence of yal_l indicates that it may contain an Alu repetitive element.
- a polynucleotide of the present invention has been identified as clone "yb8_l".
- yb8_l was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein.
- yb8_l is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as "yb8_l protein").
- nucleotide sequence of yb8_l as presently determined is reported in SEQ ID NO:19, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb8_l protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:20.
- Amino acids 69 to 81 are a predicted leader /signal sequence, with the predicted mature amino acid sequence beginning at amino acid 82. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader /signal sequence not be separated from the remainder of the yb8_l protein.
- the EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb8_l should be approximately 1800 bp.
- yb8_l demonstrated at least some similarity with sequences identified as AA418057 (zv97a06.rl Soares NhHMPu SI Homo sapiens cDNA clone 767698 5' similar to TR:G1143719 G1143719 RS-REX-B), L10334 (Homo sapiens neuroendocrine-specific protein B (NSP) mRNA, complete eds), U17603 (Rattus norvegicus rS-Rex-s mRNA, complete eds), and W19986 (zb38e09.rl Soares parathyroid tumor NbHPA Homo sapiens cDNA clone 305896 5', mRNA sequence).
- the predicted amino acid sequence disclosed herein for yb8_l was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol.
- the predicted yb8_l protein demonstrated at least some similarity to sequences identified as L10334 (neuroendocrine-specific proteins B .and C [Homo sapiens]) and U17603 (rS-Rex-s [Rattus norvegicus]). Based upon sequence similarity, yb8_l proteins and each similar protein or peptide may share at least some activity.
- the predicted yb8_l protein shows significant (60% identity) amino acid similarity to the neuro-endocrine specific protein (NSP) family of proteins. Roebroek et al. (1993, /.
- Biol Chem. 268: 13439 which is incoporated by reference herein) report observing three transcripts from this gene family: NSP-A (3.4 kb), -B (2.3 kb), and -C (1.8 kb); they encode proteins of 776, 356, and 208 amino acids, respectively. Roebroek et al. also observe that these three transcripts are identical at the 3' end and only differ over a short portion near their 5' ends, and are thus possible splice variants. NSP-A and NSP-C were found in neural and endocrine tissues while NSP-B was found only in a lung carcinoma cell line (Roebrek et al.
- the TopPredll computer program predicts two potential transmembrane domains within the yb8_l protein sequence, centered around amino acids 82 and 174 of SEQ ID NO:20, respectively.
- Clones bd306_7, fj283_ll, fk317_3, k213_2x, na316_l, nf93_20, npl64_l, pe204_l, yal_l, and yb8_l were deposited on November 26, 1997 with the American Type Culture Collection (10801 University Boulevard, Manassas, Virginia 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98599, from which each clone comprising a particular polynucleotide is obtainable.
- Clone fj283_6 was deposited on 17 November, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Virginia 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and was given the accession number ATCC xxxxx. All restrictions on the availability to the public of the deposited material will be irrevocably removed upon the granting of the patent, except for the requirements specified in 37 C.F.R. ⁇ 1.808(b), and the term of the deposit will comply with 37 C.F.R. ⁇ 1.806.
- Each clone has been transfected into separate bacterial cells (E. coli) in the accession number ATCC 98599 composite deposit. Each clone can be removed from the vector in which it was deposited by performing an EcoRI/NotI digestion (5' site, EcoRI; 3' site, NotI) to produce the appropriate fragment for such clone. Each clone was deposited in either the pED6 or pNOTs vector depicted in Figures 1A and IB, respectively.
- the pED6dpc2 vector (“pED6" was derived from pED6dpcl by insertion of a new polylinker to facilitate cDNA cloning (Kaufman et al, 1991, Nucleic Acids Res.
- the pNOTs vector was derived from pMT2 (Kaufman et ai, 1989, Mol. Cell. Biol. 9: 946-958) by deletion of the DHFR sequences, insertion of a new polylinker, and insertion of the M13 origin of replication in the Clal site.
- the deposited clone can become "flipped" (i.e., in the reverse orientation) in the deposited isolate.
- the cDNA insert can still be isolated by digestion with EcoRI and NotI.
- cDNA may also be expressed from the vectors in which they were deposited.
- Bacterial cells containing a particular clone can be obtained from the composite deposit as follows:
- oligonucleotide probe or probes should be designed to the sequence that is known for that particular clone. This sequence can be derived from the sequences provided herein, or from a combination of those sequences. The sequence of an oligonucleotide probe that was used to isolate or to sequence each full-length clone is identified below, and should be most reliable in isolating the clone of interest.
- the design of the oligonucleotide probe should preferably follow these parameters:
- the oligonucleotide should preferably be labeled with ⁇ - 32 P ATP (specific activity 6000 Ci/ mmole) and T4 polynucleotide kinase using commonly employed techniques for labeling oligonucleotides. Other labeling techniques can also be used. Unincorporated label should preferably be removed by gel filtration chromatography or other established methods. The amount of radioactivity incorporated into the probe should be quantitated by measurement in a scintillation counter. Preferably, specific activity of the resulting probe should be approximately 4e+6 dpm/pmole.
- the bacterial culture containing the pool of full-length clones should preferably be thawed and 100 ⁇ l of the stock used to inoculate a sterile culture flask containing 25 ml of sterile L-broth containing ampicillin at 100 ⁇ g/ml.
- the culture should preferably be grown to saturation at 37°C, and the saturated culture should preferably be diluted in fresh L-broth.
- Aliquots of these dilutions should preferably be plated to determine the dilution and volume which will yield approximately 5000 distinct and well-separated colonies on solid bacteriological media containing L-broth containing ampicillin at 100 ⁇ g/ml and agar at 1.5% in a 150 mm petri dish when grown overnight at 37°C. Other known methods of obtaining distinct, well-separated colonies can also be employed. Standard colony hybridization procedures should then be used to transfer the colonies to nitrocellulose filters and lyse, denature and bake them.
- the filter is then preferably incubated at 65°C for 1 hour with gentle agitation in 6X SSC (20X stock is 175.3 g NaCl/liter, 88.2 g Na citrate /liter, adjusted to pH 7.0 with NaOH) containing 0.5% SDS, 100 ⁇ g/ml of yeast RNA, and 10 mM EDTA (approximately 10 mL per 150 mm filter).
- 6X SSC 20X stock is 175.3 g NaCl/liter, 88.2 g Na citrate /liter, adjusted to pH 7.0 with NaOH) containing 0.5% SDS, 100 ⁇ g/ml of yeast RNA, and 10 mM EDTA (approximately 10 mL per 150 mm filter).
- the probe is then added to the hybridization mix at a concentration greater than or equal to le+6 dpm/mL.
- the filter is then preferably incubated at 65°C with gentle agitation overnight.
- the filter is then preferably washed in 500 mL of 2X SSC/0.5% SDS at room temperature without agitation, preferably followed by 500 mL of 2X SSC/0J% SDS at room temperature with gentle shaking for 15 minutes. A third wash with 0JX SSC/0.5% SDS at 65°C for 30 minutes to 1 hour is optional.
- the filter is then preferably dried and subjected to autoradiography for sufficient time to visualize the positives on the X-ray film. Other .known hybridization methods can also be employed.
- the positive colonies are picked, grown in culture, and plasmid DNA isolated using standard procedures.
- the clones can then be verified by restriction analysis, hybridization analysis, or DNA sequencing.
- Fragments of the proteins of the present invention which are capable of exhibiting biological activity are also encompassed by the present invention. Fragments of the protein may be in linear form or they may be cyclized using known methods, for example, as described in H.U. Saragovi, et al, Bio /Technology 10, 773-778 (1992) and in R.S.
- fragments may be fused to carrier molecules such as immunoglobulins for many purposes, including increasing the valency of protein binding sites.
- fragments of the protein may be fused through "linker" sequences to the Fc portion of an immunoglobulin.
- linker For a bivalent form of the protein, such a fusion could be to the Fc portion of an IgG molecule.
- Other immunoglobulin isotypes may also be used to generate such fusions.
- a protein - IgM fusion would generate a decavalent form of the protein of the invention.
- the present invention also provides both full-length and mature forms of the disclosed proteins.
- the full-length form of the such proteins is identified in the sequence listing by translation of the nucleotide sequence of each disclosed clone.
- the mature form(s) of such protein may be obtained by expression of the disclosed full-length polynucleotide (preferably those deposited with ATCC) in a suitable mammalian cell or other host cell.
- the sequence(s) of the mature form(s) of the protein may also be determinable from the amino acid sequence of the full-length form.
- the present invention also provides genes corresponding to the polynucleotide sequences disclosed herein.
- “Corresponding genes” are the regions of the genome that are transcribed to produce the mRNAs from which cDNA polynucleotide sequences are derived and may include contiguous regions of the genome necessary for the regulated expression of such genes. Corresponding genes may therefore include but are not limited to coding sequences, 5' and 3' untranslated regions, alternatively spliced exons, introns, promoters, enhancers, and silencer or suppressor elements. The corresponding genes can be isolated in accordance with known methods using the sequence information disclosed herein.
- Such methods include the preparation of probes or primers from the disclosed sequence information for identification and /or amplification of genes in appropriate genomic libraries or other sources of genomic materials.
- An "isolated gene” is a gene that has been separated from the adjacent coding sequences, if any, present in the genome of the organism from which the gene was isolated.
- the chromosomal location corresponding to the polynucleotide sequences disclosed herein may also be determined, for example by hybridizing appropriately labeled polynucleotides of the present invention to chromosomes in situ.
- telomere sequences may also be possible to determine the corresponding chromosomal location for a disclosed polynucleotide by identifying significantly similar nucleotide sequences in public databases, such as expressed sequence tags (ESTs), that have already been mapped to particular chromosomal locations.
- ESTs expressed sequence tags
- public database sequences having at least some similarity to the polynucleotide of the present invention have been listed by database accession number.
- the desired change in gene expression can be achieved through the use of antisense polynucleotides or nbozymes that bmd and/or cleave the mRNA transcribed from the gene (Albert and Morris, 1994, Trends Pharmacol. Sci. 15(7): 250-254; Lavarosky et al , 1997, Biochem Mol Med 62(1): 11-22; and Hampel, 1998, Prog. Nucleic Acid Res Mol. Biol. 58: 1- 39; all of which are mcorporated by reference herem).
- Transgenic ammals that have multiple copies of the gene(s) correspondmg to the polynucleotide sequences disclosed herein, preferably produced by transformation of cells with genetic constructs that are stably mamtamed within the transformed cells and their progeny, are provided.
- Transgenic animals that have modified genetic control regions that increase or reduce gene expression levels, or that change temporal or spatial patterns of gene expression, are also provided (see European Patent No. 0 649 464 Bl, incorporated by reference herein).
- organisms are provided in which the gene(s) correspondmg to the polynucleotide sequences disclosed herem have been partially or completely inactivated, through insertion of extraneous sequences into the correspondmg gene(s) or through deletion of all or part of the correspondmg gene(s).
- Partial or complete gene lnactivation can be accomplished through insertion, preferably followed by imprecise excision, of fransposable elements (Plasterk, 1992, Bwessays 14(9): 629-633, Zwaal et al , 1993, Proc Natl Acad. Sci USA 90(16). 7431-7435; Clark et al, 1994, Proc. Natl. Acad. Sci.
- Such organisms are useful for the development of non-human models for the study of disorders involving the correspondmg gene(s), and for the development of assay systems for the identification of molecules that interact with the protein product(s) of the correspondmg gene(s).
- the protein of the present invention is membrane-bound (e.g., is a receptor)
- the present invention also provides for soluble forms of such protein. In such forms, part or all of the intracellular and transmembrane domains of the protein are deleted such that the protein is fully secreted from the cell in which it is expressed.
- the intracellular and transmembr.ane domains of proteins of the invention can be identified in accordance with known techniques for determination of such domains from sequence information.
- the TopPredll computer program can be used to predict the location of transmembrane domains in an amino acid sequence, domains which are described by the location of the center of the transmsmbrane domain, with at least ten fransmembrane amino acids on each side of the reported central residue(s).
- Proteins and protein fragments of the present invention include proteins with amino acid sequence lengths that are at least 25%(more preferably at least 50%, and most preferably at least 75%) of the length of a disclosed protein and have at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% or 95% identity) with that disclosed protein, where sequence identity is determined by comparing the amino acid sequences of the proteins when aligned so as to maximize overlap and identity while minimizing sequence gaps.
- proteins and protein fragments that contain a segment preferably comprising 8 or more (more preferably 20 or more, most preferably 30 or more) contiguous amino acids that shares at least 75% sequence identity (more preferably, at least 85% identity; most preferably at least 95% identity) with any such segment of any of the disclosed proteins.
- sequence identity may be determined using WU-BLAST
- the complete suite of search programs (BLASTP, BLASTN, BLASTX, TBLASTN, and TBLASTX) is provided at that site, in addition to several support programs.
- WU-BLAST 2.0 is copyrighted and may not be sold or redistributed in any form or manner without the express written consent of the author; but the posted executables may otherwise be freely used for commercial, nonprofit, or academic purposes.
- the gapped alignment routines are integral to the database search itself, and thus yield much better sensitivity and selectivity while producing the more easily interpreted output. Gapping can optionally be turned off in all of these programs, if desired.
- the default amino acid comparison matrix is BLOSUM62, but other amino acid comparison matrices such as PAM can be utilized.
- Species homologues of the disclosed polynucleotides and proteins are also provided by the present invention.
- a "species homologue” is a protein or polynucleotide with a different species of origin from that of a given protein or polynucleotide, but with significant sequence similarity to the given protein or polynucleotide.
- polynucleotide species homologues have at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% identity) with the given polynucleotide, and protein species homologues have at least 30% sequence identity (more preferably, at least 45% identity; most preferably at least 60% identity) with the given protein, where sequence identity is determined by comparing the nucleotide sequences of the polynucleotides or the amino acid sequences of the proteins when aligned so as to maximize overlap and identity while minimizing sequence gaps.
- Species homologues may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source from the desired species.
- species homologues are those isolated from mammalian species. Most preferably, species homologues are those isolated from certain mammalian species such as, for example, Pan troglodytes, Gorilla gorilla, Pongo pygmaeus, Hylobates concolor, Macaca mulatta, Papio papio, Papio hamadryas, Cercopithecus aethiops, Cebus capucinus, Aotus trivirgatus, Sanguinus oedipus, Microcebus murinus, Mus musculus, Rattus norvegicus, Cricetulus griseus, Felis catus, Mustela vison, Canisfam ⁇ liaris, Oryctolagus cuniculus, Bos taurus, Ovis aries, Sus scrofa, and Equus caballus, for which genetic maps have been created allowing the identification of syntenic relationships between the genomic organization of genes in one species and the genomic organization of the related genes in
- allelic variants of the disclosed polynucleotides or proteins that is, naturally-occurring alternative forms of the isolated polynucleotides which also encode proteins which are identical or have significantly similar sequences to those encoded by the disclosed polynucleotides.
- allelic variants have at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% identity) with the given polynucleotide, where sequence identity is determined by comparing the nucleotide sequences of the polynucleotides when aligned so as to maximize overlap and identity while minimizing sequence gaps.
- Allelic variants may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source from individuals of the appropriate species.
- the invention also includes polynucleotides with sequences complementary to those of the polynucleotides disclosed herein.
- the present invention also includes polynucleotides that hybridize under reduced stringency conditions, more preferably stringent conditions, and most preferably highly stringent conditions, to polynucleotides described herein. Examples of stringency conditions are shown in the table below: highly stringent conditions are those that are at least as stringent as, for example, conditions A-F; stringent conditions are at least as stringent as, for example, conditions G-L; and reduced stringency conditions are at least as stringent as, for example, conditions M-R.
- the hybnd length is that anti ⁇ pated for the hybridized reg ⁇ on(s) of the hybndizing polynucleotides.
- the hybrid length is assumed to be that of the hybndizing polynucleotide.
- the hybrid length can be determined by aligning the sequences of the polynucleotides and identifying the region or regions of optimal sequence complementarity.
- SSPE lxSSPE is 0.15M NaCl, lOmM NaH 2 P0 4 , and 1.25mM EDTA, pH 7.4
- SSC 0.15M NaCl and 15mM sodium citrate
- each such hybridizing polynucleotide has a length that is at least 25%(more preferably at least 50%, and most preferably at least 75%) of the length of the polynucleotide of the present invention to which it hybridizes, and has at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% or 95% identity) with the polynucleotide of the present invention to which it hybridizes, where sequence identity is determined by comparing the sequences of the hybridizing polynucleotides when aligned so as to maximize overlap and identity while minimizing sequence gaps.
- the isolated polynucleotide of the invention may be operably linked to an expression control sequence such as the pMT2 or pED expression vectors disclosed in Kaufman et al, Nucleic Acids Res. 19, 4485-4490 (1991), in order to produce the protein recombinantly.
- an expression control sequence such as the pMT2 or pED expression vectors disclosed in Kaufman et al, Nucleic Acids Res. 19, 4485-4490 (1991)
- Many suitable expression control sequences are known in the art. General methods of expressing recombinant proteins are also known and are exemplified in R. Kaufman, Methods in Enzymology 185, 537-566 (1990).
- operably linked means that the isolated polynucleotide of the invention and an expression control sequence are situated within a vector or cell in such a way that the protein is expressed by a host cell which has been transformed (transfected) with the ligated polynucleotide/expression control sequence.
- MammaUan host cells include, for example, monkey COS cells, Chinese Hamster cells
- Ovary (CHO) cells human kidney 293 cells, human epidermal A431 cells, human Colo205 cells, 3T3 cells, CV-1 cells, other transformed primate cell lines, normal diploid cells, cell strains derived from in vitro culture of primary tissue, primary explants, HeLa cells, mouse L cells, BHK, HL-60, U937, HaK or Jurkat cells.
- yeast in lower eukaryotes such as yeast or in prokaryotes such as bacteria.
- yeast strains include Saccharomyces cerevisiae, Schizosaccharomyces pombe, Kluyveromyces strains, Candida, or any yeast strain capable of expressing heterologous proteins.
- bacterial strains include Escherichia coli, Bacillus subtilis, Salmonella typhimurium, or any bacterial strain capable of expressing heterologous proteins. If the protein is made in yeast or bacteria, it may be necessary to modify the protein produced therein, for example by phosphorylation or glycosylation of the appropriate sites, in order to obtain the functional protein. Such covalent attachments may be accomplished using known chemical or enzymatic methods.
- the protein may also be produced by operably linking the isolated polynucleotide of the invention to suitable control sequences in one or more insect expression vectors, and employing an insect expression system.
- suitable control sequences in one or more insect expression vectors, and employing an insect expression system.
- Materials and methods for baculovirus /insect cell expression systems are commercially available in kit form from, e.g., Invifrogen, San Diego, California, U.S.A. (the MaxBac® kit), and such methods are well .known in the art, as described in Summers and Smith, Texas Agricultural Experiment Station Bulletin No. 1555 (19871, incorporated herein by reference.
- an insect cell capable of expressing a polynucleotide of the present invention is "transformed.”
- the protein of the invention may be prepared by culturing transformed host cells under culture conditions suitable to express the recombinant protein.
- the resulting expressed protein may then be purified from such culture (i.e., from culture medium or cell extracts) using known purification processes, such as gel filtration and ion exchange chromatography.
- the purification of the protein may also include an affinity column containing agents which will bind to the protein; one or more column steps over such affinity resins as concanavalin A-agarose, heparin-toyopearl® or Cibacrom blue 3GA Sepharose®; one or more steps involving hydrophobic interaction chromatography using such resins as phenyl ether, butyl ether, or propyl ether; or immunoaffinity chromatography.
- the protein of the invention may also be expressed in a form which will facilitate purification.
- fusion protein such as those of maltose b.inding protein (MBP), glutathione-S-fransferase (GST) or thioredoxin (TRX). Kits for expression and purification of such fusion proteins are commercially available from New England BioLabs (Beverly, MA), Pharmacia (Piscataway, NJ) and Invifrogen Corporation (Carlsbad, CA), respectively.
- MBP maltose b.inding protein
- GST glutathione-S-fransferase
- TRX thioredoxin
- RP- HPLC reverse-phase high performance liquid chromatography
- hydrophobic RP-HPLC media e.g., silica gel having pendant methyl or other aliphatic groups
- Some or all of the foregoing purification steps, in various combinations, can also be employed to provide a substantially homogeneous isolated recombinant protein.
- the protein thus purified is substantially free of other mammalian proteins and is defined in accordance with the present invention as an "isolated protein.”
- the protein of the invention may also be expressed as a product of transgenic animals, e.g., as a component of the milk of transgenic cows, goats, pigs, or sheep which are characterized by somatic or germ cells containing a nucleotide sequence encoding the protein.
- the protein may also be produced by known conventional chemical synthesis. Methods for constructing the proteins of the present invention by synthetic means are known to those skilled in the art.
- the synthetically-constructed protein sequences by virtue of sharing primary, secondary or tertiary structural and /or conformational characteristics with proteins may possess biological properties in common therewith, including protein activity. Thus, they may be employed as biologically active or immunological substitutes for natural, purified proteins in screening of therapeutic compounds and in immunological processes for the development of antibodies.
- the proteins provided herein also include proteins characterized by amino acid sequences similar to those of purified proteins but into which modification are naturally provided or deliberately engineered. For example, modifications in the peptide or DNA sequences can be made by those skilled in the art using known techniques.
- Modifications of interest in the protein sequences may include the alteration, substitution, replacement, insertion or deletion of a selected amino acid residue in the coding sequence.
- one or more of the cysteine residues may be deleted or replaced with another amino acid to alter the conformation of the molecule.
- Techniques for such alteration, substitution, replacement, insertion or deletion are well known to those skilled in the art (see, e.g., U.S. Patent No.4,518,584).
- such alteration, substitution, replacement, insertion or deletion retains the desired activity of the protein.
- polynucleotides and proteins of the present invention are expected to exhibit one or more of the uses or biological activities (including those associated with assays cited herein) identified below.
- Uses or activities described for proteins of the present invention may be provided by administration or use of such proteins or by administration or use of polynucleotides encoding such proteins (such as, for example, in gene therapies or vectors suitable for introduction of DNA).
- the polynucleotides provided by the present invention can be used by the research community for various purposes.
- the polynucleotides can be used to express recombinant protein for analysis, characterization or therapeutic use; as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in disease states); as molecular weight markers on Southern gels; as chromosome markers or tags (when labeled) to identify chromosomes or to map related gene positions; to compare with endogenous DNA sequences in patients to identify potential genetic disorders; as probes to hybridize and thus discover novel, related DNA sequences; as a source of information to derive PCR primers for genetic fingerprinting; as a probe to "subtract-out" known sequences in the process of discovering other novel polynucleotides; for selecting and making oligomers for attachment to a "gene chip” or other support, including for examination of expression patterns; to raise anti-protein antibodies using DNA immunization techniques;
- the polynucleotide encodes a protein which binds or potentially binds to another protein (such as, for example, in a receptor-ligand interaction)
- the polynucleotide can also be used in interaction frap assays (such as, for example, those described in Gyuris et al, 1993, Cell 75: 791-803 and in Rossi et al, 1997, Proc. Natl. Acad. Sci. USA 94: 8405-8410, all of which are mcorporated by reference herein) to identify polynucleotides encoding the other protein with which binding occurs or to identify inhibitors of the binding interaction.
- the proteins provided by the present invention can similarly be used in assay to determine biological activity, including in a panel of multiple proteins for high- throughput screening; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its receptor) in biological fluids; as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state); and, of course, to isolate correlative receptors or ligands.
- the protein binds or potentially binds to another protein (such as, for example, in a receptor-ligand interaction)
- the protein can be used to identify the other protein with which binding occurs or to identify inhibitors of the binding interaction. Proteins involved in these binding interactions can also be used to screen for peptide or small molecule inhibitors or agonists of the binding interaction.
- Polynucleotides and proteins of the present invention can also be used as nutritional sources or supplements. Such uses include without limitation use as a protein or amino acid supplement, use as a carbon source, use as a nitrogen source and use as a source of carbohydrate.
- the protein or polynucleotide of the invention can be added to the feed of a particular organism or can be administered as a separate solid or liquid preparation, such as in the form of powder, pills, solutions, suspensions or capsules.
- the protein or polynucleotide of the invention can be added to the medium in or on which the microorganism is cultured.
- a protein of the present invention may exhibit cytokine, cell proliferation (either inducing or inhibiting) or cell differentiation (either inducing or inhibiting) activity or may induce production of other cytokines in certain cell populations.
- cytokine cytokine
- cell proliferation either inducing or inhibiting
- cell differentiation either inducing or inhibiting
- the activity of a protein of the present invention is evidenced by any one of a number of routine factor dependent cell proliferation assays for cell lines including, without limitation, 32D, DA2, DA1G, T10, B9, B9/11, BaF3, MC9/G, M+ (preB M+), 2E8, RB5, DAI, 123, T1165, HT2, CTLL2, TF-1, Mo7e and CMK.
- the activity of a protein of the invention may, among other means, be measured by the following methods:
- Assays for T-cell or thymocyte proliferation include without limitation those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A.M. Kruisbeek, D.H. Margulies, E.M. Shevach, W Strober, Pub. Greene Publishing Associates and Wiley- Interscience (Chapter 3, In Vitro assays for Mouse Lymphocyte Function 3.1-3.19; Chapter 7, Immunologic studies in Humans); Takai et al., J. Immunol. 137:3494-3500, 1986; Bertagnolli et al., J. Immunol.
- Assays for cytokine production and /or proliferation of spleen cells, lymph node cells or thymocytes include, without limitation, those described in: Polyclonal T cell stimulation, Kruisbeek, A.M. and Shevach, E.M. In Current Protocols in Immunology. J.E.e.a. Coligan eds. Vol 1 pp. 3.12.1-3.12.14, John Wiley and Sons, Toronto. 1994; and Measurement of mouse and human Interferon ⁇ , Schreiber, R.D. In Current Protocols in Immunology. J.E.e.a. Coligan eds. Vol 1 pp. 6.8.1-6.8.8, John Wiley and Sons, Toronto. 1994.
- Assays for proliferation and differentiation of hematopoietic and lymphopoietic cells include, without limitation, those described in: Measurement of Human and Murine Interleukin 2 and Interleukin 4, Bottomry, K., Davis, L.S. and Lipsky, P.E. In Current Protocols in Immunology. J.E.e.a. Coligan eds. Vol 1 pp. 6.3.1-6.3.12, John Wiley and Sons, Toronto. 1991; deVries et al., J. Exp. Med. 173:1205-1211, 1991; Moreau et al., Nature 336:690-692, 1988; Greenberger et al., Proc. Natl. Acad. Sci. U.S.A. 80:2931-2938, 1983;
- a protein of the present invention may also exhibit immune stimulating or immune suppressing activity, including without limitation the activities for which assays are described herein.
- a protein may be useful in the treatment of various immune deficiencies and disorders (including severe combined immunodeficiency (SCID)), e.g., in regulating (up or down) growth and proliferation of T and/or B lymphocytes, as well as effecting the cytolytic activity of NK cells and other cell populations.
- SCID severe combined immunodeficiency
- These immune deficiencies may be genetic or be caused by viral (e.g., HIV) as well as bacterial or fungal infections, or may result from autoimmune disorders.
- infectious diseases causes by viral, bacterial, fungal or other infection may be treatable using a protein of the present invention, including infections by HIV, hepatitis viruses, herpesviruses, mycobacteria, Leishmania spp., malaria spp. and various fungal infections such as candidiasis.
- a protein of the present invention may also be useful where a boost to the immune system generally may be desirable, i.e., in the treatment of cancer.
- Autoimmune disorders which may be treated using a protein of the present invention include, for example, connective tissue disease, multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, autoimmune pulmonary inflammation, Guillain-Barre syndrome, autoimmune thyroiditis, insulin dependent diabetes mellitis, myasthenia gravis, graft-versus-host disease and autoimmune inflammatory eye disease.
- a protein of the present invention may also to be useful in the treatment of allergic reactions and conditions, such as asthma (particularly allergic asthma) or other respiratory problems.
- Other conditions, in which immune suppression is desired may also be freatable using a protein of the present invention.
- T cells may be inhibited by suppressing T cell responses or by inducing specific tolerance in T cells, or both.
- Immunosuppression of T cell responses is generally an active, non-antigen-specific, process which requires continuous exposure of the T cells to the suppressive agent.
- Tolerance which involves inducing non-responsiveness or anergy in T cells, is distinguishable from immunosuppression in that it is generally antigen-specific and persists after exposure to the tolerizing agent has ceased. Operationally, tolerance can be demonstrated by the lack of a T cell response upon reexposure to specific antigen in the absence of the tolerizing agent.
- Down regulating or preventing one or more antigen functions (including without limitation B lymphocyte antigen functions (such as , for example, B7)), e.g., preventing high level lymphokine synthesis by activated T cells, will be useful in situations of tissue, skin and organ transplantation and in graft-versus-host disease (GVHD).
- B lymphocyte antigen functions such as , for example, B7
- GVHD graft-versus-host disease
- blockage of T cell function should result in reduced tissue destruction in tissue transplantation.
- rejection of the transplant is initiated through its recognition as foreign by T cells, followed by an immune reaction that destroys the transplant.
- a molecule which inhibits or blocks interaction of a B7 lymphocyte antigen with its natural ligand(s) on immune cells such as a soluble, monomeric form of a peptide having B7-2 activity alone or in conjunction with a monomeric form of a peptide having an activity of another B lymphocyte antigen (e.g., B7- 1, B7-3) or blocking antibody), prior to transplantation can lead to the binding of the molecule to the natural ligand(s) on the immune cells without transmitting the corresponding costimulatory signal.
- Blocking B lymphocyte antigen function in this matter prevents cytokine synthesis by immune cells, such as T cells, and thus acts as an immunosuppressant.
- the lack of costimulation may also be sufficient to anergize the T cells, thereby inducing tolerance in a subject.
- Induction of long-term tolerance by B lymphocyte antigen-blocking reagents may avoid the necessity of repeated administration of these blocking reagents.
- the efficacy of particular blocking reagents in preventing organ transplant rejection or GVHD can be assessed using animal models that are predictive of efficacy in humans.
- appropriate systems which can be used include allogeneic cardiac grafts in rats and xenogeneic pancreatic islet cell grafts in mice, both of which have been used to examine the immunosuppressive effects of CTLA4Ig fusion proteins in vivo as described in Lenschow et al, Science 257:789-792 (1992) and Turka et al, Proc. Natl. Acad. Sci USA, 89:11102-11105 (1992).
- murine models of GVHD see Paul ed., Fundamental Immunology, Raven Press, New York, 1989, pp. 846-847) can be used to determine the effect of blocking B lymphocyte antigen function in vivo on the development of that disease.
- Blocking antigen function may also be therapeutically useful for treating autoimmune diseases.
- Many autoimmune disorders are the result of inappropriate activation of T cells that are reactive against self tissue and which promote the production of cytokines and autoantibodies involved in the pathology of the diseases.
- Preventing the activation of autoreactive T cells may reduce or eliminate disease symptoms.
- Administration of reagents which block costimulation of T cells by disrupting recepto ⁇ ligand interactions of B lymphocyte antigens can be used to inhibit T cell activation and prevent production of autoantibodies or T cell-derived cytokines which may be involved in the disease process.
- blocking reagents may induce antigen-specific tolerance of autoreactive T cells which could lead to long-term relief from the disease.
- the efficacy of blocking reagents in preventing or alleviating autoimmune disorders can be determined using a number of well-characterized animal models of human autoimmune diseases. Examples include murine experimental autoimmune encephalitis, systemic lupus erythmatosis in MKL/lpr/lpr mice or NZB hybrid mice, murine autoimmune collagen arthritis, diabetes mellitus in NOD mice and BB rats, and murine experimental myasthenia gravis (see Paul ed., Fundamental Immunology, Raven Press, New York, 1989, pp. 840-856).
- Upregulation of an antigen function (preferably a B lymphocyte antigen function), as a means of up regulating immune responses, may also be useful in therapy. Upregulation of immune responses may be in the form of enhancing an existing immune response or eliciting an initial immune response. For example, enhancing an immune response through stimulating B lymphocyte antigen function may be useful in cases of viral infection. In addition, systemic viral diseases such as influenza, the common cold, and encephalitis might be alleviated by the administration of stimulatory forms of B lymphocyte antigens systemically.
- anti-viral immune responses may be enhanced in an infected patient by removing T cells from the patient, costimulating the T cells in vitro with viral antigen- pulsed APCs either expressing a peptide of the present invention or together with a stimulatory form of a soluble peptide of the present invention and reintroducing the in vitro activated T cells into the patient.
- Another method of enhancing anti-viral immune responses would be to isolate infected cells from a patient, transfect them with a nucleic acid encoding a protein of the present invention as described herein such that the cells express all or a portion of the protein on their surface, and reintroduce the transfected cells into the patient.
- the infected cells would now be capable of delivering a costimulatory signal to, and thereby activate, T cells in vivo.
- up regulation or enhancement of antigen function may be useful in the induction of tumor immunity.
- Tumor cells e.g., sarcoma, melanoma, lymphoma, leukemia, neuroblastoma, carcinoma
- fransfected with a nucleic acid encoding at least one peptide of the present invention can be administered to a subject to overcome tumor-specific tolerance in the subject. If desired, the tumor cell can be transfected to express a combination of peptides.
- tumor cells obtained from a patient can be transfected ex vivo with an expression vector directing the expression of a peptide having B7-2-like activity alone, or in conjunction with a peptide having B7-l-like activity and /or B7-3-like activity.
- the fransfected tumor cells are returned to the patient to result in expression of the peptides on the surface of the transfected cell.
- gene therapy techniques can be used to target a tumor cell for transfection in vivo.
- tumor cells which lack MHC class I or MHC class II molecules, or which fail to reexpress sufficient amounts of MHC class I or MHC class II molecules, can be transfected with nucleic acid encoding all or a portion of (e.g., a cytoplasmic-domain truncated portion) of an MHC class I chain protein and ⁇ 2 microglobulin protein or an MHC class II ⁇ chain protein and an MHC class II ⁇ chain protein to thereby express MHC class I or MHC class II proteins on the cell surface.
- nucleic acid encoding all or a portion of (e.g., a cytoplasmic-domain truncated portion) of an MHC class I chain protein and ⁇ 2 microglobulin protein or an MHC class II ⁇ chain protein and an MHC class II ⁇ chain protein to thereby express MHC class I or MHC class II proteins on the cell surface.
- a gene encoding an antisense construct which blocks expression of .an MHC class II associated protein, such as the invariant chain can also be cotransfected with a DNA encoding a peptide having the activity of a B lymphocyte antigen to promote presentation of tumor associated antigens and induce tumor specific immunity.
- a T cell mediated immune response in a human subject may be sufficient to overcome tumor-specific tolerance in the subject.
- Suitable assays for thymocyte or splenocyte cytotoxicity include, without limitation, those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A.M. Kruisbeek, D.H. Margulies, E.M. Shevach, W Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 3, In Vitro assays for Mouse Lymphocyte Function 3.1- 3.19; Chapter 7, Immunologic studies in Humans); Herrmann et al., Proc. Natl. Acad. Sci. USA 78:2488-2492, 1981; Herrmann et al., J. Immunol. 128:1968-1974, 1982; Handa et al.,
- T-cell-dependent immunoglobulin responses and isotype switching include, without limitation, those described in: Maliszewski, J. Immunol. 144:3028-3033, 1990; and Assays for B cell function: In vitro antibody production, Mond, J.J. and Brunswick, M. In Current Protocols in Immunology. J.E.e.a. Coligan eds. Vol 1 pp. 3.8.1-3.8.16, John Wiley and Sons, Toronto. 1994.
- MLR Mixed lymphocyte reaction
- Dendritic cell-dependent assays (which will identify, among others, proteins expressed by dendritic cells that activate naive T-cells) include, without limitation, those described in: Guery et al., J. Immunol.
- lymphocyte survival /apoptosis (which will identify, among others, proteins that prevent apoptosis after superantigen induction and proteins that regulate lymphocyte homeostasis) include, without limitation, those described in: Darzynkiewicz et al., Cytometiy 13:795-808, 1992; Gorczyca et al, Leukemia 7:659-670, 1993; Gorczyca et al., Cancer Research 53:1945-1951, 1993; Itoh et al., Cell 66:233-243, 1991; Zacharchuk, Journal of Immunology 145:4037-4045, 1990; Zamai et al., Cytometiy 14:891-897, 1993; Gorczyca et al., international Journal of Oncology 1:639-648, 1992.
- Assays for proteins that influence early steps of T-cell commitment and development include, without limitation, those described in: Antica et al., Blood 84:111-117, 1994; Fine et al., Cellular Immunology 155:111-122, 1994; Galy et al., Blood 85:2770-2778, 1995; Toki et al., Proc. Nat. Acad Sci. USA 88:7548-7551, 1991.
- a protein of the present invention may be useful in regulation of hematopoiesis and, consequently, in the treatment of myeloid or lymphoid cell deficiencies. Even marginal biological activity in support of colony forming cells or of factor-dependent cell lines indicates involvement in regulating hematopoiesis, e.g.
- erythroid progenitor cells alone or in combination with other cytokines, thereby indicating utility, for example, in treating various anemias or for use in conjunction with irradiation /chemotherapy to stimulate the production of erythroid precursors .and/or erythroid cells; in supporting the growth and proliferation of myeloid cells such as granulocytes and monocytes /macrophages (i.e., traditional CSF activity) useful, for example, in conjunction with chemotherapy to prevent or treat consequent myelo-suppression; in supporting the growth and proliferation of megakaryocytes and consequently of platelets thereby allowing prevention or treatment of various platelet disorders such as thrombocytopenia, and generally for use in place of or complimentary to platelet transfusions; and /or in supporting the growth and proliferation of hematopoietic stem cells which are capable of maturing to any and all of the above- mentioned hematopoietic cells and therefore find therapeutic utility in various stem cell disorders (such as those usually
- the activity of a protein of the invention may, among other means, be measured by the following methods:
- Assays for proliferation and differentiation of various hematopoietic lines are cited above.
- Assays for embryonic stem cell differentiation (which will identify, among others, proteins that influence embryonic differentiation hematopoiesis) include, without limitation, those described in: Johansson et al. Cellular Biology 15:141-151, 1995; Keller et al., Molecular and Cellular Biology 13:473-486, 1993; McClanahan et al., Blood 81:2903-2915, 1993.
- Assays for stem cell survival and differentiation include, without limitation, those described in: Methylcellulose colony forming assays, Freshney, M.G.
- a protein of the present invention also may have utility in compositions used for bone, cartilage, tendon, ligament and /or nerve tissue growth or regeneration, as well as for wound healing and tissue repair and replacement, and in the treatment of burns, incisions .and ulcers.
- a protein of the present invention which induces cartilage and /or bone growth in circumstances where bone is not normally formed, has application in the healing of bone fractures and cartilage damage or defects in humans and other animals.
- Such a preparation employing a protein of the invention may have prophylactic use in closed as well as open fracture reduction and also in the improved fixation of artificial joints.
- De novo bone formation induced by an osteogenic agent contributes to the repair of congenital, trauma induced, or oncologic resection induced craniofacial defects, and also is useful in cosmetic plastic surgery.
- a protein of this invention may also be used in the treatment of periodontal disease, and in other tooth repair processes.
- Such agents may provide an environment to attract bone-forming cells, stimulate growth of bone-forming cells or induce differentiation of progenitors of bone-forming cells.
- a protein of the invention may also be useful in the treatment of osteoporosis or osteoarthritis, such as through stimulation of bone and /or cartilage repair or by blocking inflammation or processes of tissue destruction (collagenase activity, osteoclast activity, etc.) mediated by inflammatory processes.
- tissue regeneration activity that may be attributable to the protein of the present invention is tendon /ligament formation.
- a protein of the present invention which induces tendon/ligament-like tissue or other tissue formation in circumstances where such tissue is not normally formed, has application in the healing of tendon or ligament tears, deformities and other tendon or ligament defects in humans and other animals.
- Such a preparation employing a tendon /ligament-like tissue inducing protein may have prophylactic use in preventing damage to tendon or ligament tissue, as well as use in the improved fixation of tendon or ligament to bone or other tissues, and in repairing defects to tendon or ligament tissue.
- compositions of the present invention contributes to the repair of congenital, trauma induced, or other tendon or ligament defects of other origin, and is also useful in cosmetic plastic surgery for attachment or repair of tendons or ligaments.
- the compositions of the present invention may provide an environment to attract tendon- or ligament-forming cells, stimulate growth of tendon- or ligament-forming cells, induce differentiation of progenitors of tendon- or ligament-forming cells, or induce growth of tendon/ligament cells or progenitors ex vivo for return in vivo to effect tissue repair.
- the compositions of the invention may also be useful in the treatment of tendinitis, carpal tunnel syndrome and other tendon or ligament defects.
- the compositions may also include an appropriate matrix and /or sequestering agent as a carrier as is well known in the art.
- the protein of the present invention may also be useful for proliferation of neural cells and for regeneration of nerve and brain tissue, i.e. for the treatment of cenfral and peripheral nervous system diseases and neuropathies, as well as mechanical and traumatic disorders, which involve degeneration, death or trauma to neural cells or nerve tissue. More specifically, a protein may be used in the treatment of diseases of the peripheral nervous system, such as peripheral nerve injuries, peripheral neuropathy and localized neuropathies, and central nervous system diseases, such as Alzheimer's, Parl nson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Shy-Drager syndrome. Further conditions which may be treated in accordance with the present invention include mechanical and traumatic disorders, such as spinal cord disorders, head trauma and cerebrovascular diseases such as stroke. Peripheral neuropathies resulting from chemotherapy or other medical therapies may also be treatable using a protein of the invention.
- Proteins of the invention may also be useful to promote better or faster closure of non-healing wounds, including without limitation pressure ulcers, ulcers associated with vascular insufficiency, surgical and traumatic wounds, and the like. It is expected that a protein of the present invention may also exhibit activity for generation or regeneration of other tissues, such as organs (including, for example, pancreas, liver, intestine, kidney, skin, endothelium), muscle (smooth, skeletal or cardiac) and vascular (including vascular endothelium) tissue, or for promoting the growth of cells comprising such tissues. Part of the desired effects may be by inhibition or modulation of fibrotic scarring to allow normal tissue to regenerate. A protein of the invention may also exhibit angiogenic activity.
- organs including, for example, pancreas, liver, intestine, kidney, skin, endothelium
- muscle smooth, skeletal or cardiac
- vascular including vascular endothelium
- a protein of the present invention may also be useful for gut protection or regeneration and treatment of lung or liver fibrosis, reperfusion injury in various tissues, and conditions resulting from systemic cytokine damage.
- a protein of the present invention may also be useful for promoting or inhibiting differentiation of tissues described above from precursor tissues or cells; or for inhibiting the growth of tissues described above.
- the activity of a protein of the invention may, among other means, be measured by the following methods:
- Assays for tissue generation activity include, without limitation, those described in: International Patent Publication No. WO95/ 16035 (bone, cartilage, tendon); International Patent Publication No. WO95/05846 (nerve, neuronal); International Patent Publication No. WO91/07491 (skin, endothelium ).
- Assays for wound healing activity include, without limitation, those described in:
- a protein of the present invention may also exhibit activin- or inhibin-related activities. Inhibins are characterized by their ability to inhibit the release of follicle stimulating hormone (FSH), while activins and are characterized by their ability to stimulate the release of follicle stimulating hormone (FSH).
- FSH follicle stimulating hormone
- a protein of the present invention alone or in heterodimers with a member of the inhibin ⁇ family, may be useful as a contraceptive based on the ability of inhibins to decrease fertility in female mammals and decrease spermatogenesis in male mammals. Administration of sufficient amounts of other inhibins can induce infertility in these mammals.
- the protein of the invention may be useful as a fertiUty inducing therapeutic, based upon the abiUty of activin molecules in stimulating FSH release from ceUs of the anterior pituitary. See, for example, United States Patent 4,798,885.
- a protein of the invention may also be useful for advancement of the onset of fertiUty in sexuaUy immature mammals, so as to increase the lifetime reproductive performance of domestic animals such as cows, sheep and pigs.
- the activity of a protein of the invention may, among other means, be measured by the following methods:
- Assays for activin/inhibin activity include, without limitation, those described in: Vale et al., Endocrinology 91:562-572, 1972; Ling et al., Nature 321:779-782, 1986; Vale et al., Nature 321:776-779, 1986; Mason et al., Nature 318:659-663, 1985; Forage et al., Proc. Natl. Acad. Sci. USA 83:3091-3095, 1986.
- a protein of the present invention may have chemotactic or chemokinetic activity (e.g., act as a chemokine) for mammalian cells, including, for example, monocytes, fibroblasts, neutrophils, T-ceUs, mast cells, eosinophils, epitheUal and/or endothelial ceUs.
- Chemotactic and chemokinetic proteins can be used to mobilize or attract a desired cell population to a desired site of action.
- Chemotactic or chemokinetic proteins provide particular advantages in treatment of wounds and other trauma to tissues, as well as in freatment of localized infections. For example, attraction of lymphocytes, monocytes or neutrophils to tumors or sites of infection may result in improved immune responses against the tumor or infecting agent.
- a protein or peptide has chemotactic activity for a particular cell population if it can stimulate, directly or indirectly, the directed orientation or movement of such cell population.
- the protein or peptide has the abiUty to directly stimulate directed movement of ceUs. Whether a particular protein has chemotactic activity for a population of cells can be readily determined by employing such protein or peptide in any known assay for cell chemotaxis.
- the activity of a protein of the invention may, among other means, be measured by the following methods:
- Assays for chemotactic activity consist of assays that measure the ability of a protein to induce the migration of ceUs across a membrane as weU as the abiUty of a protein to induce the adhesion of one cell population to another cell population.
- Suitable assays for movement and adhesion include, without Umitation, those described in: Current Protocols in Immunology, Ed by
- a protein of the invention may also exhibit hemostatic or thrombolytic activity.
- such a protein is expected to be useful in treatment of various coagulation disorders (including hereditary disorders, such as hemophiUas) or to enhance coagulation and other hemostatic events in treating wounds resulting from trauma, surgery or other causes.
- a protein of the invention may also be useful for dissolving or inhibiting formation of thromboses and for treatment and prevention of conditions resulting therefrom (such as, for example, infarction of cardiac and central nervous system vessels (e.g., stroke).
- the activity of a protein of the invention may, among other means, be measured by the following methods: Assay for hemostatic and thrombolytic activity include, without limitation, those described in: Linet et al., J. Clin. Pharmacol. 26:131-140, 1986; Burdick et al., Thrombosis Res.45:413-419, 1987; Humphrey et al., Fibrinolysis 5:71-79 (1991); Schaub, Prostaglandins 35:467-474, 1988.
- a protein of the present invention may also demonstrate activity as receptors, receptor ligands or inhibitors or agonists of receptor/ligand interactions.
- receptors and ligands include, without limitation, cytokine receptors and their ligands, receptor kinases and their ligands, receptor phosphatases and their ligands, receptors involved in ceU-ceU interactions and their Ugands (including without Umitation, cellular adhesion molecules (such as selectins, integrins and their ligands) and receptor/ligand pairs involved in antigen presentation, antigen recognition and development of ceUular and humoral immune responses).
- Receptors and Ugands are also useful for screening of potential peptide or small molecule inhibitors of the relevant receptor/ligand interaction.
- a protein of the present invention including, without
- Umitation, fragments of receptors and ligands may themselves be useful as inhibitors of receptor/ligand interactions.
- Suitable assays for receptor-ligand activity include without limitation those described in:Current Protocols in Immunology, Ed by J.E. Coligan, A.M. Kruisbeek, D.H. Margulies, E.M. Shevach, W.Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 7.28, Measurement of Cellular Adhesion under static conditions 7.28.1-7.28.22), Takai et al, Proc. Natl. Acad. Sci. USA 84:6864-6868, 1987; Bierer et al, J. Exp. Med.
- Proteins of the present invention may also exhibit anti-inflammatory activity.
- the anti-inflammatory activity may be achieved by providing a stimulus to cells involved in the inflammatory response, by inhibiting or promoting cell-cell interactions (such as, for example, cell adhesion), by inhibiting or promoting chemotaxis of cells involved in the inflammatory process, inhibiting or promoting cell extravasation, or by stimulating or suppressing production of other factors which more directly inhibit or promote an inflammatory response.
- Proteins exhibiting such activities can be used to treat inflammatory conditions including chronic or acute conditions), including without Umitation inflammation associated with infection (such as septic shock, sepsis or systemic inflammatory response syndrome (SIRS)), ischemia-reperfusion injury, endotoxin lethality, arthritis, complement-mediated hyperacute rejection, nephritis, cytokine or chemokine-induced lung injury, inflammatory bowel disease, Crohn's disease or resulting from over production of cytol ines such as TNF or IL-1. Proteins of the invention may also be useful to treat anaphylaxis and hypersensitivity to an antigenic substance or material.
- Umitation inflammation associated with infection such as septic shock, sepsis or systemic inflammatory response syndrome (SIRS)
- ischemia-reperfusion injury such as septic shock, sepsis or systemic inflammatory response syndrome (SIRS)
- ischemia-reperfusion injury such as septic shock, sepsis or systemic
- Cadherins are calcium-dependent adhesion molecules that appear to play major roles during development, particularly in defining specific cell types. Loss or alteration of normal cadherin expression can lead to changes in cell adhesion properties linked to tumor growth and metastasis. Cadherin malfunction is also implicated in other human diseases, such as pemphigus vulgaris and pemphigus foliaceus (auto-immune blistering skin diseases), Crohn's disease, and some developmental abnormalities.
- the cadherin superfamily includes well over forty members, each with a distinct pattern of expression. All members of the superfamily have in common conserved extracellular repeats (cadherin domains), but structural differences are found in other parts of the molecule.
- the cadherin domains bind calcium to form their tertiary structure and thus calcium is required to mediate their adhesion. Only a few amino acids in the first cadherin domain provide the basis for homophilic adhesion; modification of this recognition site can change the specificity of a cadherin so that instead of recognizing only itself, the mutant molecule can now also bind to a different cadherin. In addition, some cadherins engage in heterophilic adhesion with other cadherins.
- E-cadherin one member of the cadherin superfamily, is expressed in epitheUal ceU types. Pathologically, if E-cadherin expression is lost in a tumor, the malignant cells become invasive and the cancer metastasizes. Transfection of cancer cell lines with polynucleotides expressing E-cadherin has reversed cancer-associated changes by returning altered ceU shapes to normal, restoring ceUs' adhesiveness to each other and to their substrate, decreasing the cell growth rate, and drastically reducing anchorage- independent cell growth. Thus, reinfroducing E-cadherin expression reverts carcinomas to a less advanced stage. It is likely that other cadherins have the same invasion suppressor role in carcinomas derived from other tissue types.
- proteins of the present invention with cadherin activity and polynucleotides of the present invention encoding such proteins, can be used to treat cancer. Introducing such proteins or polynucleotides into cancer ceUs can reduce or eUminate the cancerous changes observed in these cells by providing normal cadherin expression.
- Cancer cells have also been shown to express cadherins of a different tissue type than their origin, thus allowing these cells to invade and metastasize in a different tissue in the body.
- Proteins of the present invention with cadherin activity, and polynucleotides of the present invention encoding such proteins, can be substituted in these cells for the inappropriately expressed cadherins, restoring normal cell adhesive properties and reducing or eliminating the tendency of the cells to metastasize.
- proteins of the present invention with cadherin activity can be used to generate antibodies recognizing and binding to cadherins.
- Such antibodies can be used to block the adhesion of inappropriately expressed tumor-cell cadherins, preventing the cells from forming a tumor elsewhere.
- Such an anti-cadherin antibody can also be used as a marker for the grade, pathological type, and prognosis of a cancer, i.e. the more progressed the cancer, the less cadherin expression there wiU be, and this decrease in cadherin expression can be detected by the use of a cadherin-binding antibody.
- Fragments of proteins of the present invention with cadherin activity can also be used to block cadherin function by binding to cadherins and preventing them from binding in ways that produce undesirable effects.
- fragments of proteins of the present invention with cadheirin activity preferably truncated soluble cadherin fragments which have been found to be stable in the circulation of cancer patients, and polynucleotides encoding such protein fragments, can be used to disturb proper cell-cell adhesion.
- Assays for cadherin adhesive and invasive suppressor activity include, without limitation, those described in: Hortsch et al. J Biol Chem 270 (32): 18809-18817, 1995; Miyaki et al. Oncogene 11: 2547-2552, 1995; Ozawa et al. Cell 63: 1033-1038, 1990.
- a protein of the invention may exhibit other anti-tumor activities.
- a protein may inhibit tumor growth directly or indirectly (such as, for example, via antibody-dependent ceU-mediated cytotoxicity (ADCC)).
- a protein may exhibit its tumor inhibitory activity by acting on tumor tissue or tumor precursor tissue, by inhibiting formation of tissues necessary to support tumor growth (such as, for example, by inhibiting angiogenesis), by causing production of other factors, agents or cell types which inhibit tumor growth, or by suppressing, eliminating or inhibiting factors, agents or cell types which promote tumor growth.
- a protein of the invention may also exhibit one or more of the following additional activities or effects: inhibiting the growth, infection or function of, or killing, infectious agents, including, without Umitation, bacteria, viruses, fungi and other parasites; effecting (suppressing or enhancing) bodily characteristics, including, without limitation, height, weight, hair color, eye color, skin, fat to lean ratio or other tissue pigmentation, or organ or body part size or shape (such as, for example, breast augmentation or diminution, change in bone form or shape); effecting biorhythms or caricadic cycles or rhythms; effecting the fertility of male or female subjects; effecting the metabolism, catabolism, anabolism, processing, utilization, storage or elimination of dietary fat, lipid, protein, carbohydrate, vitamins, minerals, cofactors or other nutritional factors or component(s); effecting behavioral characteristics, including, without limitation, appetite, libido, stress, cognition (including cognitive disorders), depression (including depressive disorders) and violent behaviors; providing analgesic effects or other pain reducing effects;
- a protein of the present invention may be used in a pharmaceutical composition when combined with a pharmaceutically acceptable carrier.
- a pharmaceutically acceptable carrier may also contain (in addition to protein and a carrier) diluents, fillers, salts, buffers, stabilizers, solubilizers, and other materials weU known in the art.
- pharmaceutically acceptable means a non-toxic material that does not interfere with the effectiveness of the biological activity of the active ingredient(s). The characteristics of the carrier will depend on the route of administration.
- the pharmaceutical composition of the invention may also contain cytokines, lymphokines, or other hematopoietic factors such as M-CSF, GM-CSF, TNF, IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IFN, TNFO, TNF1, TNF2, G-CSF, Meg-CSF, thrombopoietin, stem ceU factor, and erythropoietin.
- the pharmaceutical composition may further contain other agents which either enhance the activity of the protein or compliment its activity or use in treatment.
- protein of the present invention may be included in formulations of the particular cytokine, lymphokine, other hematopoietic factor, thrombolytic or anti-thrombotic factor, or anti-inflammatory agent to minimize side effects of the cytokine, lymphokine, other hematopoietic factor, thrombolytic or anti-thrombotic factor, or anti-inflammatory agent.
- a protein of the present invention may be active in multimers (e.g., heterodimers or homodimers) or complexes with itself or other proteins.
- compositions of the invention may comprise a protein of the invention in such multimeric or complexed form.
- the pharmaceutical composition of the invention may be in the form of a complex of the protein(s) of present invention along with protein or peptide antigens.
- the protein and /or peptide antigen wtil deliver a stimulatory signal to both B and T lymphocytes.
- B lymphocytes wiU respond to antigen through their surface immunoglobulin receptor.
- T lymphocytes will respond to antigen through the T cell receptor (TCR) following presentation of the antigen by MHC proteins.
- TCR T cell receptor
- MHC and structurally related proteins including those encoded by class I and class II MHC genes on host cells will serve to present the peptide antigen(s) to T lymphocytes.
- antigen components could also be supplied as purified MHC-peptide complexes alone or with co-stimulatory molecules that can directly signal T ceUs.
- antibodies able to bind surface immunolgobulin and other molecules on B cells as well as antibodies able to bind the TCR and other molecules on T cells can be combined with the pharmaceutical composition of the invention.
- the pharmaceutical composition of the invention may be in the form of a liposome in which protein of the present invention is combined, in addition to other pharmaceutically acceptable carriers, with amphipathic agents such as lipids which exist in aggregated form as micelles, insoluble monolayers, liquid crystals, or lamellar layers in aqueous solution.
- Suitable Upids for liposomal formulation include, without Umitation, monoglycerides, diglycerides, sulfatides, lysolecithin, phospholipids, saponin, bile acids, and the like. Preparation of such Uposomal formulations is within the level of skill in the art, as disclosed, for example, in U.S. Patent No. 4,235,871; U.S. Patent No. 4,501,728; U.S.
- the term "therapeutically effective amount” means the total amount of each active component of the pharmaceutical composition or method that is sufficient to show a meaningful patient benefit, i.e., treatment, healing, prevention or amelioration of the relevant medical condition, or an increase in rate of freatment, healing, prevention or amelioration of such conditions.
- a therapeutically effective amount of protein of the present invention is administered to a mammal having a condition to be treated.
- Protein of the present invention may be administered in accordance with the method of the invention either alone or in combination with other therapies such as treatments employing cytokines, lymphokines or other hematopoietic factors.
- protein of the present invention may be administered either simultaneously with the cytokine(s), lymphokine(s), other hematopoietic factor(s), thrombolytic or anti-thrombotic factors, or sequentially. If administered sequentially, the attending physician will decide on the appropriate sequence of administering protein of the present invention in combination with cytoakine(s), lymphokine(s), other hematopoietic factor(s), thrombolytic or anti-thrombotic factors.
- Administration of protein of the present invention used in the pharmaceutical composition or to practice the method of the present invention can be carried out in a variety of conventional ways, such as oral ingestion, inhalation, topical application or cutaneous, subcutaneous, intraperitoneal, parenteral or intravenous injection. Intravenous administration to the patient is preferred.
- protein of the present invention When a therapeutically effective amount of protein of the present invention is administered orally, protein of the present invention will be in the form of a tablet, capsule, powder, solution or eUxir.
- the pharmaceutical composition of the invention may additionaUy contain a solid carrier such as a gelatin or an adjuvant.
- the tablet, capsule, and powder contain from about 5 to 95% protein of the present invention, and preferably from about 25 to 90% protein of the present invention.
- a liquid carrier such as water, petroleum, oils of animal or plant origin such as peanut oil, mineral oil, soybean oil, or sesame oil, or synthetic oils may be added.
- the liquid form of the pharmaceutical composition may further contain physiological saline solution, dexfrose or other saccharide solution, or glycols such as ethylene glycol, propylene glycol or polyethylene glycol.
- the pharmaceutical composition When administered in Uquid form, contains from about 0.5 to 90% by weight of protein of the present invention, and preferably from about 1 to 50% protein of the present invention.
- protein of the present invention wiU When a therapeutically effective amount of protein of the present invention is administered by intravenous, cutaneous or subcutaneous injection, protein of the present invention wiU be in the form of a pyrogen-free, parenterally acceptable aqueous solution.
- the preparation of such parenterally acceptable protein solutions having due regard to pH, isotonicity, stability, and the like, is within the skill in the art.
- a preferred pharmaceutical composition for intravenous, cutaneous, or subcutaneous injection should contain, in addition to protein of the present invention, an isotonic vehicle such as Sodium Chloride Injection, Ringer's Injection, Dextrose Injection, Dexfrose and Sodium Chloride Injection, Lactated Ringer's Injection, or other vehicle as known in the art.
- an isotonic vehicle such as Sodium Chloride Injection, Ringer's Injection, Dextrose Injection, Dexfrose and Sodium Chloride Injection, Lactated Ringer's Injection, or other vehicle as known in the art.
- the pharmaceutical composition of the present invention may also contain stabilizers, preservatives, buffers, antioxidants, or other additives known to those of skill in the art.
- the amount of protein of the present invention in the pharmaceutical composition of the present invention wiU depend upon the nature and severity of the condition being treated, and on the nature of prior treatments which the patient has undergone. Ultimately, the attending physician will decide the amount of protein of the present invention with which to treat each individual patient. Initially, the attending physician will administer low doses of protein of the present invention and observe the patient's response. Larger doses of protein of the present invention may be administered until the optimal therapeutic effect is obtained for the patient, and at that point the dosage is not increased further.
- compositions used to practice the method of the present invention should contain about 0.01 ⁇ g to about 100 mg (preferably about OJng to about 10 mg, more preferably about 0J ⁇ g to about 1 mg) of protein of the present invention per kg body weight.
- the duration of intravenous therapy using the pharmaceutical composition of the present invention will vary, depending on the severity of the disease being freated and the condition and potential idiosyncratic response of each individual patient. It is contemplated that the duration of each application of the protein of the present invention will be in the range of 12 to 24 hours of continuous intravenous administration. Ultimately the attending physician will decide on the appropriate duration of intravenous therapy using the pharmaceutical composition of the present invention.
- Protein of the invention may also be used to immunize animals to obtain polyclonal and monoclonal antibodies which specifically react with the protein. Such antibodies may be obtained using either the entire protein or fragments thereof as an immunogen.
- the peptide immunogens additionally may contain a cysteine residue at the carboxyl terminus, and are conjugated to a hapten such as keyhole limpet hemocyanin (KLH).
- KLH keyhole limpet hemocyanin
- Monoclonal antibodies binding to the protein of the invention may be useful diagnostic agents for the immunodetection of the protein.
- Neutralizing monoclonal antibodies binding to the protein may also be useful therapeutics for both conditions associated with the protein and also in the freatment of some forms of cancer where abnormal expression of the protein is involved.
- neutralizing monoclonal antibodies against the protein may be useful in detecting and preventing the metastatic spread of the cancerous cells, which may be mediated by the protein.
- the therapeutic method includes administering the composition topically, systematically, or locally as an implant or device.
- the therapeutic composition for use in this invention is, of course, in a pyrogen-free, physiologically acceptable form.
- the composition may desirably be encapsulated or injected in a viscous form for delivery to the site of bone, cartilage or tissue damage.
- Topical administration may be suitable for wound healing and tissue repair.
- Therapeutically useful agents other than a protein of the invention which may also optionally be included in the composition as described above, may alternatively or additionally, be administered simultaneously or sequentially with the composition in the methods of the invention.
- the composition would include a matrix capable of delivering the protein-containing composition to the site of bone and /or cartilage damage, providing a structure for the developing bone and cartilage and optimally capable of being resorbed into the body.
- Such matrices may be formed of materials presently in use for other implanted medical applications.
- compositions may be biodegradable and chemically defined calcium sulfate, tricalciumphosphate, hydroxyapatite, polylactic acid, polyglycolic acid and polyanhydrides.
- potential materials are biodegradable and biologically well- defined, such as bone or dermal collagen.
- Further matrices are comprised of pure proteins or extraceUular matrix components.
- Other potential matrices are nonbiodegradable and chemically defined, such as sintered hydroxapatite, bioglass, aluminates, or other ceramics.
- Matrices may be comprised of combinations of any of the above mentioned types of material, such as polylactic acid and hydroxyapatite or collagen and tricalciumphosphate.
- the bioceramics may be altered in composition, such as in calcium- aluminate-phosphate and processing to alter pore size, particle size, particle shape, and biodegradability.
- a 50:50 (mole weight) copolymer of lactic acid and glycolic acid in the form of porous particles having diameters ranging from 150 to 800 microns.
- a sequestering agent such as carboxymethyl cellulose or autologous blood clot, to prevent the protein compositions from disassociating from the matrix.
- a preferred family of sequestering agents is cellulosic materials such as alkylcelluloses (including hydroxyalkylcelluloses), including methylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropyl- methylcellulose, and carboxymethylcellulose, the most preferred being cationic salts of carboxymethylceUulose (CMC).
- Other preferred sequestering agents include hyaluronic acid, sodium alginate, poly(ethylene glycol), polyoxyethylene oxide, carboxyvinyl polymer and poly(vinyl alcohol).
- the amount of sequestering agent useful herein is 0.5-20 wt%, preferably 1-10 wt% based on total formulation weight, which represents the amount necessary to prevent desorbtion of the protein from the polymer matrix and to provide appropriate handling of the composition, yet not so much that the progenitor cells are prevented from infiltrating the matrix, thereby providing the protein the opportunity to assist the osteogenic activity of the progenitor cells.
- proteins of the invention may be combined with other agents beneficial to the treatment of the bone and /or cartilage defect, wound, or tissue in question. These agents include various growth factors such as epidermal growth factor (EGF), platelet derived growth factor (PDGF), transforming growth factors (TGF- and TGF- ⁇ ), and insulin-like growth factor (IGF).
- EGF epidermal growth factor
- PDGF platelet derived growth factor
- TGF- and TGF- ⁇ transforming growth factors
- IGF insulin-like growth factor
- the dosage regimen of a protein-containing pharmaceutical composition to be used in tissue regeneration will be determined by the attending physician considering various factors which modify the action of the proteins, e.g., amount of tissue weight desired to be formed, the site of damage, the condition of the damaged tissue, the size of a wound, type of damaged tissue (e.g., bone), the patient's age, sex, and diet, the severity of any infection, time of administration and other clinical factors.
- the dosage may vary with the type of matrix used in the reconstitution and with inclusion of other proteins in the pharmaceutical composition.
- the addition of other known growth factors, such as IGF I (insulin Uke growth factor I) may also effect the dosage.
- Progress can be monitored by periodic assessment of tissue /bone growth and /or repair, for example, X-rays, histomorphomefric determinations and tefracycline labeling.
- Polynucleotides of the present invention can also be used for gene therapy. Such polynucleotides can be introduced either in vivo or ex vivo into cells for expression in a mammaUan subject. Polynucleotides of the invention may also be administered by other known methods for introduction of nucleic acid into a ceU or organism (including, without limitation, in the form of viral vectors or naked DNA).
- Cells may also be cultured ex vivo in the presence of proteins of the present invention in order to proUferate or to produce a desired effect on or activity in such cells. Treated cells can then be introduced in vivo for therapeutic purposes.
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Abstract
Description
Claims
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6680497P | 1997-11-26 | 1997-11-26 | |
US66804P | 1997-11-26 | ||
US19788698A | 1998-11-23 | 1998-11-23 | |
US197886 | 1998-11-23 | ||
PCT/US1998/025149 WO1999026961A1 (en) | 1997-11-26 | 1998-11-24 | Secreted proteins and polynucleotides encoding them |
Publications (2)
Publication Number | Publication Date |
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EP1040118A1 true EP1040118A1 (en) | 2000-10-04 |
EP1040118A4 EP1040118A4 (en) | 2003-04-09 |
Family
ID=26747164
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP98959599A Withdrawn EP1040118A4 (en) | 1997-11-26 | 1998-11-24 | Secreted proteins and polynucleotides encoding them |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1040118A4 (en) |
JP (1) | JP2002506611A (en) |
AU (1) | AU1536399A (en) |
CA (1) | CA2311683A1 (en) |
WO (1) | WO1999026961A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US20010039335A1 (en) * | 1997-04-10 | 2001-11-08 | Kenneth Jacobs | Secreted proteins and polynucleotides encoding them |
FR2804962B1 (en) * | 2000-02-10 | 2005-02-25 | Aventis Pharma Sa | PARTNERS OF THE PTB1 DOMAIN OF FE65, PREPARATION AND USES |
DK1257642T3 (en) | 2000-02-10 | 2009-03-30 | Aventis Pharma Sa | Partners for the PTB1 domain of FE65, manufacturing and applications |
US6774209B1 (en) | 2000-04-03 | 2004-08-10 | Dyax Corp. | Binding peptides for carcinoembryonic antigen (CEA) |
-
1998
- 1998-11-24 EP EP98959599A patent/EP1040118A4/en not_active Withdrawn
- 1998-11-24 CA CA002311683A patent/CA2311683A1/en not_active Abandoned
- 1998-11-24 AU AU15363/99A patent/AU1536399A/en not_active Abandoned
- 1998-11-24 JP JP2000522118A patent/JP2002506611A/en not_active Withdrawn
- 1998-11-24 WO PCT/US1998/025149 patent/WO1999026961A1/en not_active Application Discontinuation
Non-Patent Citations (6)
Title |
---|
CASTAGNOLA P ET AL: "Cartilage associated protein (CASP) is a novel developmentally regulated chick embryo protein." JOURNAL OF CELL SCIENCE. ENGLAND JUN 1997, vol. 110 ( Pt 12), June 1997 (1997-06), pages 1351-1359, XP002222438 ISSN: 0021-9533 -& DATABASE EMBL [Online] 30 April 1996 (1996-04-30) retrieved from EMBL Database accession no. X97607 XP002222642 * |
DATABASE EMBL [Online] 30 June 1996 (1996-06-30) retrieved from EMBL Database accession no. W51808 XP002222440 * |
JACOBS K A ET AL: "A genetic selection for isolating cDNA clones that encode signal peptides." METHODS IN ENZYMOLOGY. UNITED STATES 1999, vol. 303, 1999, pages 468-479, XP001119908 ISSN: 0076-6879 * |
JACOBS K A ET AL: "A GENETIC SELECTION FOR ISOLATING CDNAS ENCODING SECRETED PROTEINS" GENE: AN INTERNATIONAL JOURNAL ON GENES AND GENOMES, ELSEVIER SCIENCE PUBLISHERS, BARKING, GB, vol. 198, 1 October 1997 (1997-10-01), pages 289-296, XP002924016 ISSN: 0378-1119 * |
See also references of WO9926961A1 * |
TONACHINI L ET AL: "cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP)." CYTOGENETICS AND CELL GENETICS. SWITZERLAND 1999, vol. 87, no. 3-4, 1999, pages 191-194, XP009001861 ISSN: 0301-0171 -& DATABASE EMBL [Online] 16 October 2001 (2001-10-16) retrieved from EMBL Database accession no. O75718 XP002222643 -& DATABASE EMBL [Online] 17 June 1998 (1998-06-17) retrieved from EMBL Database accession no. AJ006470 XP002222644 * |
Also Published As
Publication number | Publication date |
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WO1999026961A1 (en) | 1999-06-03 |
AU1536399A (en) | 1999-06-15 |
EP1040118A4 (en) | 2003-04-09 |
JP2002506611A (en) | 2002-03-05 |
CA2311683A1 (en) | 1999-06-03 |
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