CA1339642C - Recombinant purified protease nexin - Google Patents

Abstract

DNA segments encoding two slightly different protease nexin I forms (PN-I.alpha. and PN-I.beta.) are cloned and expressed to provide practical quantities of PN-I
for diagnostic and therapeutic use. PN-I is a serine protease inhibitor useful in controlling conditions mediated by proteolytic activity.

Description

-1- 13~642 RECOMBINANT PURIFIED PROTEASE NEXIN

Technical Field The invention relates to recombinant production of protein~ affecting the cardiovascular system. In particular, it concerns the cloning and expression of genes encoding forms of protease nexin I (PN~

Backqround Art Connective tissue cells secrete protease inhibitors which are specific for serine proteafies.
Since serine proteases are involved in development and migration of cells, regulation of the activity of these enzymes is necessary to exercise control over the remodeling or destruction of tissues (Proteases in Bioloqical Control (1975), Reich, E., et al, eds., Cold Spring Harbor, New York). The inhibitors designated protease nexins irreversibly bind to serine proteases at their catalytic sites (Baker, J.B., et al, Cell (1980) 21:37-45) and effect the clearance of the bound proteases via receptor-mediated endo~ytosis and lysosomal degradation (Low, ~.A., et al, Proc Natl Acad Sci (USA) (1981) 78:2340-2344: Ba~er, J.B., et al, in The Receptors 3 (1985), *

13~Y~'~2 Three ~rotease nexins have been identified.
Protease nexin I (PN-I) has been purified from serum-free medium conditioned by human foreskin cells (Scott, R.W., et al, J Biol Chem (1983) 58:10439-10444). It is a 43 kd glycoprotein which is released byfibroblasts, myotubes, heart muscle cells, and vascular smooth muscle cells. Its release, along with that of plasminogen activator, is stimulated by phorbol esters and by mitogens (Eaton, D.L., et al, J Cell Biol (1983) 123:128). Native PN-I is an approximately 400 amino acid protein containing about 6% carbohydrate. Since it is present only in trace levels in serum, it ap~arently functions at or near the surfaces of interstitial cells. PN-I inhibits all the known acti~ators of urokinase eroenzyme, plasmin, trypsin, thrombin, and factor Xa (Eaton, D.L., et al, J Biol Chem (1984) 259:6241). It also inhibits tissue plasminogen activator and urokinase.
A protein called neurite-~romoting factor (NPF) has also been reported to be isolated from glioma cells, to have a 43 kd molecular weight, and to inhibit proteolysis catalyzed by urokinase or plasminogen activator (Guenther. J., et al, EMB0 Journal (1985) 4:1963-1966). It was first reported as inducing neurite outgrowth in neuroblastoma cells (Barde, Y.A.. et al, Nature (1978) 274:818). The amino acid sequence of this protein, but not the sequence of the CDNA encoding it, is disclosed in Gloor, S., et al, Cell (1986) 47:687-693. Any relationship between this DNA and those reported herein is uncertain, since the restriction map for the glial CDNA clearly differs from that of the cDNAs disclosed herein. The NPF protein is a 379 amino l~g642 acid sequence preceded by an 18 amino acid, met-preceded signal. It differs from the PN-I~ disclosed herein at amino acid position 241 of the mature protein.
The need for practical amounts of purified PN-I
is severalfold. First, PN-I has clear utility as a pharmaceutical for conditions characterized by excess amounts of urokinase and tissue plasminogen activator, or as an antidote for overdoses of these enzymes as agents for solution of blood clots. Indications which are clearly susceptible to PN-I treatment include the autoimmune disease penphigus, which is commonly encountered in dogs, and psoriasis, which is believed to be due to an overproduction of plasminogen activator.
Second, because the role of PN-I in regulating various developmental stages of tissue formation and remodeling is relatively com~lex, it would be desirable to be able to use model systems to discern in greater detail the role PN-I plays. This can be done effectively only if practical quantities are available. Finally, PN-I is useful as an assay reagent in immunological assays for its levels in serum or in other tissues or for other biological assays.
Exemplary of the conditions for which further study of the role of PN-I is desirable are tumor metastasis, wound healing, and inflammation. In tumor metastasis, malignant cells must penetrate the extracellular matrix laid down by vascular smooth muscle cells, a process which is mediated by secreted plasminogen activator. In the model system of Jones, P.A., et al, Cancer Res (1980) 40:3222, an in vitro system based on the invasion of the extracellular mat~ix by human fibrosarcoma cells, it could be shown that PN-I
at 0.1 ~M causes virtually complete su~pression of the invasion (Bergman, B.L., et al, Proc Natl Acad Sci USA

1~3964~, (1986) 83:996-1000). The proteolytic activity of thrombin, which is a fibroblast mitogen important in wound healing, is effective only when added to cultures at concentrations above the concentrations of secreted PN-I (Baker, J.B., et al, J Cell PhYsiol (1982) 112:291;
Low, D.A., et al, Nature (1982) 298: 2476). It has been suggested that PN-I has an anti-inflammatory function, since PN-I secretion by synovial fibroblasts increases dramatically when the cells are treated with interleukin-I.
PN-I may also have a neurological function, since the above-mentioned similar protease inhibitor stimulates neurite extension (Monard et al, Proq Brain Res (1983) 58:359)-Elucidation of the precise function of PN-I in any of the foregoing would be greatly simplified by the availability of the needed amounts of pure material.
These amounts are also needed for use in PN-I as a pharmaceutical and in diagnosis and assay. The present invention provides a solution to the problem of obtaining sufficient quantities of PN-I, as well as a mechanism for modifying PN-I structure in order to make it more effective.

Disclosure of the Invention The invention provides a highly purified PN-I
protein, including recombinant forms, and the DNA coding sequences, expression systems, and methods which permit the production of recombinant mammalian PN-I. Two exemplary forms of PN-I are disclosed.
By employing these materials and methods, desired quantities of the PN-I protein can be produced, either in glycosylated or unglycosylated form, depending on the expression systems employed, and the gene can be i3~Y~2 modified, if desired, to alter the precise amino acid sequence so afi to enhance the desired properties of the protein. This is all possible through the availability of genes encodinq human PN-I, which are directly useful in producing the corresponding PN-I, and are also useful as probes to retrieve cDNA sequences encoding these genes in a variety of species.
The human genes encoding two closely related PN-I proteins are illustrated below. Retrieval of PN-I
encoding DNA of other species is also desirable: that encoding the murine protein(s) is particularly desirable, as many model systems for providing a detailed description of the role of such factors are conveniently based on murine cells, tissues, or whole organisms.
Thus, in one aspect the invention relates to DNA sequences encoding mammalian PN-I and to derivatives thereof, which can be expressed to obtain proteins with PN-I activity. In other aspects, the invention relates to cells transformed with these DNA sequences, and to the PN-I proteins produced by these cells. In addition, the invention relates to purified protein having the N-terminal sequence of the native protein as disclosed herein, to antibodies prepared by administration of the recombinant or purified native protein, and to DNA
probes capable of retrieving PN-I cDNA.

Brief Description of the Drawinqs Figures la and lb show the sequences of two probe mixtures which were employed in the illustration below to identify PN-I clones.
Figure 2 shows restriction maps of the cDN~
clones designated PN-9 (representative of the class to which PN-33 belongs) and PN-18, each of which contains the coding sequence for a complete PN-I protein.

i 3 ~ Y 6 .t 2 Figure 3 shows the nucleotide sequence of the coding region of PN-18 and the deduced amino acid sequence of PN-Ia.
Figure 4 shows the nucleotide sequence of the 5 coding region of PN-33 and the deduced amino acid sequence of PN-I~.
Figure 5 shows a Northern blot of mRNA extracts from several cell lines using a Sau3AI fragment from PN-18 as a probe.
Figure 6 shows the splice junction region of the PN-I gene which accounts for the production of the PN-Ia and PN-IB forms.
Figure 7 shows the expression vector pSNH-dhfr.

15 Modes of carrYinq Out the Invention A. Definitions As used herein, ~protease nexin I~ (PN-I) refers to a protein which is active in the standard 20 diagnostic assays for PN-I, which are based on four criteria, as follows: (1) The protein complexes to thrombin: (2) this complexation is accelerated by heparin; (3) the protein binds to the cell of its origin, for example, in the illustration below, to 25 fibroblasts: and (4) heparin must inhibit this binding.
PN-I is distinguishable from the two other protease nexin factors, PN-II and PN-III (Knauer, D.J., et al, J Biol Chem (1982) 257:15098-15104), which are also major thrombin inhibitors, but are less strongly 30 binding to this protease.
~ Control sequence~ refers to a DNA sequence or sequences which are capable, when properly ligated to a desired coding sequence, of effecting its expression in hosts compatible with such sequences. Such control sequences include at least promoters in both procaryotic _7_ ~3 3 and eucaryotic host6, and preferably, transcription termination signals. Additional factors neces6ary or helpful in effecting expression may also be identified.
As used herein, ~control sequences~ simply refers to whatever DNA sequence may be required to effect expres6ion in the particular host used.
''Cells~ or "cell cultures~ or ~recombinant host cells'l or ~host cells'l are often used interchangeably as will be clear from the context. These terms include the immediate subject cell, and, of course, the progeny thereof. It is understood that not all progeny are exactly identical to the parental cell, due to chance mutations or differences in environment. However, such altered progeny are included in these terms, so long as the progeny retain the characteristics relevant to those conferred on the originally transformed cell. In the present case, for example, such a characteristic might be the ability to produce recombinant PN-I.
~Purifiedll or "pure" refers to material which is free from substances which normally accompany it as found in its native state. Thus "pure" PN-I-encoding DNA refers to DNA which is found in isolation from its native environment and free of association with DNAs encoding other proteins normally produced by cells natively producing PN-I. ''Purell PN-I refers to PN-I
which does not contain materials normally associated with its in situ environment in human or other mammalian tissue. Of course, "pure" PN-I may include materials in covalent as60ciation with it, such as glycoside residues or materials introduced for, for example, formulation as a therapeutic. ~Pure~ simply designates a situation wherein the substance referred to is, or has been, isolated from its native environment and materials which normally accompany it.

-8- 133~42 Of course, the DNA claimed herein as purified and free of substances normally accompanying it, but encoding PN-I, can include additional sequence at the 5' and/or 3' end of the coding sequence which might result, for example, from reverse transcription of the noncoding portions of the message when the DNA is derived from a cDNA library or might include the reverse transcript for the signal sequence as well as the mature protein encoding sequence.
"Degenerate with~, as referced to a DNA
sequence, refers to nucleotide sequences encoding the same amino acid sequence as that referenced.
"Operably linked'l refers to a juxtaposition wherein the components are configured so as to perform their usual function. Thus, control sequences or promoters operably linked to a coding sequence are capable of effecting the expression of the coding sequence.

B. General DescriPtion PN-I was purified to homogeneity from serum-free medium conditioned by human foreskin fibroblasts in microcarrier cultures by affinity chromatography on heparin-agarose, followed by gel-exclusion chromatography, as described in detail byScott, R.W., et al, J Biol Chem (1985) 260:7029-7034, Of course, other chromatographic supports which contain heparin for affinity binding can also be used. The purified protein shows an Mr of 42-43 kd, based on sedimentation equilibrium analysis, or of 47 kd, estimated from gel-exclusion chromatography. The purified material shows the properties exhibited by PN-I when contained in conditioned medium, including formation of sodium 1339~2 dodecylsulfate-6table complexes with thrombin, urokinase, and plafimin; inhibition of proteafie activity;
heparin-enhanced inhibition of thrombin and cellular binding of protease-PN complexes in a heparin-sensitive reaction. The purified native protein contains approximately 6% carbohydrate with 2.3% amino sugar, 1.1% neutral sugar, and 3.0% fiialic acid. The N-terminal amino acid sequence of the isolated, purified protease nexin was determined for the first 34 amino ~~ acids to be: Ser-Hifi-Phe-Asn-Pro-Leu-Ser-Leu-Glu-Glu-Leu-Gly-Ser-Asn-Thr-Gly-Ile-Gln-~al-Phe-Asn-Gln-Ile-~al-Lys-Ser-Arg-Pro-His-Asp-Afin-Ile-Val-Ile.
cDNA encoding the complete human PN-I protein was obtained from a foreskin fibroblast DNA library.
The retrieval of this clone took advantage of probes based on the amino acid sequence determined in the native protein. The cloned cDNA is amenable to expression in recombinant cells of both procaryotic and eucaryotic organisms, as described above, by excising the coding sequence from the carrier vector and ligating it into suitable expresfiion systems. The PN-I can be directly produced as a mature protein preceded by a Met N-terminal amino acid (which may or may not be processed, depending on the choice of expression systems) may be produced as a fusion protein to any desirable additional N-terminal or C-terminal sequence, or may be secreted as a mature protein when preceded by a signal sequence, either its own, or a heterologous sequence provided by, for example, the known signal sequence asfiociated with the bacterial ~-lactamase gene or with secreted human genes such as insulin or growth hormones. Means for providing suitable restriction sites at appropriate locations with respect to the desired coding sequence by site-directed mutagenesis are ~39~2 well understood, and the coding sequence can thus be provided with suitable sites for attachment to signal sequence or fusion sequence, or into expression vectors.
If bacterial hosts are chosen, it is likely that the protein will be produced in nonglycosylated form. If the PN-l is produced intracellularly as a "mature" protein, the N-terminal methionine may be only partially processed, or not processed at all. Thus, the protein produced may include the N-terminal met.
Modification of the erotein produced either intracellularly or as secreted from such bacterial host can be done by providing the polysaccharide substances, by refolding using techniques to sever and reform disulfide bonds, or other post-translational ex vivo processing techniques. If the protein is produced in mammalian or other eucaryotic hosts, the cellular environment is such that post-translational processing can occur in vivo, and a glycosylated form of the protein is produced.
The recombinant cells are cultured under conditions suitable for the host in question, and the protein is recovered from the cellular lysate or from the medium, as determined by mode of expression.
Purification of the protein can be achieved using methods similar to that disclosed by Scott, R.W., et al, J Biol Chem (supra), or by other means known in the art.
The purified protein is then formulated according to its application. For pharmaceutical applications, the protein is formulated into compositions using standard excipients, as is understood by practitioners of the art, and disclosed, for example, in Reminqton's Pharmaceutical Sciences, latest edition, Mack Publishing Company, Easton, PA. If to be used in diagnostic or immunoassay, the protein may be labeled 3 g ~ '1 2 using radioacti~e species, for example, or fluorescent markers. If it is to be used to obtain antibody preparations, the protein is prepared for injection along with suitable adjuvant. Methods of modifying the recombinant protein of the invention according to its desired use will be clear from the generally practiced techniques of the art.
Two forms of PN-I, PN-Ia and PN-I~ are illustrated below. They are highly homologous and contain 378 and 379 amino acids, respectively in the mature sequence, differing only at position 310 where the Arg of PN-Ia is replaced by Thr-Gly in PN-I~.
Both have a 19 amino acid signal beginning at Met. The location of the N-terminus is deduced from the sequenced native protein and it is highly likely this is correct;
however, there is a small probability that alternate processing site(s) may also be utilized.

C. Standard Methods Most of the techniques which are used to transform cells, construct vectors, extract messenger RNA, prepare cDNA libraries, and the like are widely practiced in the art, and most practitioners are familiar with the standard resource materials which describe specific conditions and procedures. However, for convenience, the following paragraphs may serve as a guideline.

C.l. Hosts and Control Sequences Both procaryotic and eucaryotic systems may be used to express the PN-I encoding sequences of the invention; procaryotic hosts are, of course, the most convenient for cloning procedures. Procaryotes most frequently are represented by various strains of E

1339~i42 coli however, other microbial strains may also be used. Plasmid vectors which contain replication sites, selectable markers and control sequences derived from a species compatible with the host are used; for example, E. coli is typically transformed using derivatives of pBR3Z2, a plasmid derived from an E. coli species by Bolivar, et al, Gene (1977) 2:95. pBR322 contains genes for ampicillin and tetracycline resistance, and thus provides multiple selectable markers which can be eit~er retained or destroyed in constructing the desired vector. Commonly used procaryotic control sequences which are defined herein to include promoters for transcription initiation, optionally with an operator, along with ribosome binding site sequences, include such commonly used promoters as the ~-lactamase (penicillinase) and lactose (lac) promoter systems (Chang, et al, Nature (1977) 198:1056) and the tryptophan (trp) promoter system (G~eddel, et al Nucleic Acids Res (1980) 8:4057) and the lambda-derived PL
promoter and N-gene ribosome binding site (shimatake~ et al, Nature (1981) 292:128).
In addition to bacteria, eucaryotic microbes, such as yeast, may also be used as hosts. Laboratory strains of Saccharomyces cerevisiae, Baker's yeast, are most used although a number of other strains or species are commonly available. ~ectors employing, for example, the 2 ~ origin of replication of Broach, J. R., Meth Enz (1983) 101:307, or other yeast compatible origins of replication (see, for example, Stinchcomb, et al, Nature (1979) 282:39, Tschum~er, G., et al, Gene (1980) 10:157 and Clarke, L, et al, Meth Enz (1983) 101:300) may be used. Control sequences for yeast vectors include promoters for the synthesis of glycolytic enzymes (Hess, et al, J Adv Enzyme Req (1968) 7:149; Holland, et al, i~3~42 Biochemistry (1978) 17:4900). Additional promoters . .
known in the art include the promoter for 3-phosphoglycerate kinase (Hitzeman, et al, J Biol Chem (1980) 255:2073). Other promoters, which have the additional advantage of transcription controlled by growth conditions and/or genetic background are the promoter regions for alcohol dehydrogenase 2, isocytochrome C, acid phosphatase, degradative enzymes associated with nitrogen metabolism, the alpha factor system and enzymes res~onsible for maltose and galactose utilization. It is also believed terminator sequences are desirable at the 3l end of the coding sequences.
Such terminators are found in the 3' untranslated region following the coding sequences in yeast-derived genes.
It is also, of course, possible to express genes encoding polypeptides in eucaryotic host cell cultures derived from multicellular organisms. See, for examele, Axel, et al, U.S. Patent No. 4,399,216. These systems have the additional advantage of the ability to splice out introns and thus can be used directly to express genomic fragments. Useful host cell lines include VERO and HeLa cells, and Chinese hamster ovary (CHO) cells. Ex~ression vectors for such cells ordinarily include promoters and control sequences compatible with mammalian cells such as, for example, the commonly used early and late promoters from Simian Virus 40 (SV 40) (Fiers, et al, Nature (1978) 273:113), or other viral promoters such as those derived from polyoma, Adenovirus 2, bovine papilloma virus, or avian sarcoma viruses. The controllable promoter, hMTII
(Karin, M., et al, Nature (1982) 299:797-802) may also be used. General aspects of mammalian cell host system transformations have been described by Axel (supra). It now appears, also that ~enhancer~ regions are important -14- 1~ ~ gtJ4 2 in optimizing expression: these are, generally, sequences found u~stream or downstream of the promoter region in noncoding DNA regions. Origins of replication may be obtained, if needed, from viral sources.
However, integration into the chromosome i6 a common mechanism for DNA replication in eucaryotes.

C.2. Transformations Depending on the host cell used, transformation is done using standard techniques appropriate to such cells. The calcium treatment employing calcium chloride, as described by Cohen, S.N., Proc Natl Acad Sci (USA) (1972) 69:2110, or the RbC12 method described in Maniatis, et al, Molecular Cloninq: A
Laboratory Manual (1982) Cold Spring Harbor Press, p.
254 and Hanahan, D., J Mol Biol (1983) 166:557_580 may be used for procaryotes or other cells which contain substantial cell wall barriers. For mammalian cells without such cell walls, the calcium phosphate precipitation method of Graham and van der Eb, ViroloqY
(1978) 52:546, optionally as modified by Wigler, M., et al, Cell (1979) 16:777_785 may be used. Transformations into yeast may be carried out according to the method of Beggs, J.D., Nature (1978) 275:104-109 or of Hinnen, A., et al, Proc Natl Acad Sci (USA) (1978) 75:1929.

C.3. Vector Construction Construction of suitable vectors containing the desired coding and control sequences employs standard ligation and restriction techniques which are well understood in the art. Isolated plasmids, DNA
sequences, or synthesized oligonucleotides are cleaved, tailored, and religated in the form desired.

- 13~642 The DNA sequences which form the vectors are available from a number of source6. Backbone vectors and control systems are generally found on available ~host" vectors which are used for the bulk of the sequences in construction. Typical sequences have been set forth in llC .1 above. For the pertinent coding sequence, initial construction may be, and usually is, a matter of retrieving the appropriate sequences from cDNA
or genomic DNA libraries. However, once the sequence is disclosed it is possible to synthesize the entire gene sequence in vitro starting from the individual nucleoside derivatives. The entire gene sequence for genes of sizeable length, e.g., 500-1000 bp may be prepared by synthesizing individual overlapping complementary oligonucleotides and filling in single stranded nonoverlapping portions using DNA polymerase in the presence of the deoxyribonucleotide triphosphates.
This approach has been used successfully in the construction of several genes of known fiequence. See, for example, Edge, M. D., Nature (1981) 292:756;
Nambair, K. P., et al, Science (1984) 223:1299: Jay, Ernest, J Biol Chem (1984) 259:6311.
Synthetic oligonucleotides are prepared by either the phosphotriester method as described by Edge, et al, Nature (supra) and Duckworth, et al, Nucleic Acids Res (1981) 9:1691 or the phosphoramidite method as described by Beaucage, S.L., and Caruthers, M.H., Tet Letts (1981) 22:1859 and Matteucci. M.D., and Caruthers, M.H., J Am Chem Soc (1981) 103:3185 and can be prepared using commercially available automated oligonucleotide synthesizers. Kinasing of single strands prior to annealing or for labeling is achieved using an excess, e.g., approximately 10 units of polynucleotide kinase to 1 nmole substrate in the presence of 50 mM Tris, pH 7.6, 1339~42 10 mM MgC12, 5 mM dithiothreitol, 1-2 mM ATP, 1.7 pmoles y32P-ATP (2.9 mCi/mmole), 0.1 mM spermidine, O.1 mM EDTA.
Once the components of the desired vectors are thus available, they can be excised and ligated using standard restriction and ligation procedures.
Site specific DNA cleavage is performed by treating with the suitable restriction enzyme (or enzymes) under conditions which are generally understood in the art, and the particulars of which are specified by the manufacturer of these commercially available restriction enzymes. See, e.g., New England Biolabs, Product Catalog. In general, about 1 ~g of plasmid or DNA sequence is cleaved by one unit of enzyme in about 20 ~1 of buffer solution: in the examples herein, typically, an excess of restriction enzyme is used to insure complete digestion of the DNA substrate.
Incubation times of about one hour to two hours at about 37~C are workable, although variations can be tolerated. After each incubation, protein is removed by extraction with phenol/chloroform, and may be followed by ether extraction, and the nucleic acid recovered from aqueous fractions by precipitation with ethanol. If desired, size separation of the cleaved fragments may be performed by polyacrylamide gel or agarose gel electrophoresis using standard techniques. A general description of size separations is found in Methods in EnzYmoloqy (1980) 65:499-560.
Restriction cleaved fragments may be blunt ended by treating with the large fragment of E. coli DNA
polymerase I (Klenow) in the presence of the four deoxynucleotide triphosphates (dNTPs) using incubation times of about 15 to 25 min at 20 to 25~C in 50 mM Tris pH 7.6, 50 mM NaCl, 6 mM MgC12, 6 mM DTT and 0.1-1.0 13~g642 mM dNTPs. The Klenow fragment fills in at 5' single-stranded overhangs but chews back protruding 3' single strands, even though the four dNTPs are present.
If desired, selective repair can be performed by supplying only one of the, or selected, dNTPs within the limitations dictated by the nature of the overhang.
After treatment with Klenow, the mixture is extracted with phenol/chloroform and ethanol erecipitated.
Treatment under appropriate conditions with Sl nuclease or BAL-31 results in hydrolysis of any single-stranded portion.
Ligations are performed in 15-50 ~1 volumes under the following standard conditions and temperatures: for example, 20 mM Tris-Cl pH 7.5, 10 mM
MgC12, 10 mM DTT, 33 ~g/ml BSA, 10 mM-50 mM NaCl, and either 40 ~M ATP, 0.01-0.02 (Weiss) units T4 DNA
ligase at 0~C (for "sticky end~ ligation) or 1 mM ATP, 0.3-0.6 (Weiss) units T4 DN~ ligase at 14~C (for llblunt end'l ligation). Intermolecular ~sticky end~ ligations are usually performed at 33-100 ~g/ml total DNA
concentrations (5-100 n~ total end concentration).
Intermolecular blunt end ligations are performed at 1 ~M total ends concentration.
In vector construction employing ~vector fragments", the vector fragment is commonly treated with bacterial alkaline phosphatase (BAP) or calf intestinal alkaline phosphatase (CIP) in order to remove the 5' phosphate and prevent self-ligation of the vector.
Digestions are conducted at pH 8 in approximately 10 mM
Tris-HCl, 1 mM EDTA using about 1 unit of BAP or CIP per ~g of vector at 60~ for about one hour. In order to recover the nucleic acid fragments, the preparation is extracted with phenol/chloroform and ethanol precipitated. Alternatively, religation can be prevented in vectors which have been double digested by additional restriction enzyme digestion and separation of the unwanted fragments.
~or portions of vectors derived from cDNA or genomic DNA which require sequence modifications, site specific primer directed mutagenesis may ~e used (Zoller, M.J., and Smith, M. Nucleic Acids Res (1982) 10:6487-6500 and Adelman, J.P., et al, DNA (1983) 2:183-193). This is conducted using a primer synthetic oligonucleotide complementary to a single stranded phage DNA to be mutagenized except for limited mismatching, representing the desired mutation. Briefly, the synthetic oligonucleotide is used as a primer to direct synthesis of a strand complementary to the phage, and the resulting partially or fully double-stranded DNA is transformed into a phage-supporting host bacterium.
Cultures of the transformed bacteria are plated in top agar, permitting plaque formation from single cells which harbor the phage.
Theoretically, 50% of the new plaques will contain the phage having, as a single strand, the mutated form: 50% will have the original sequence. The resulting plaques are washed after hybridization with kinased synthetic primer at a wash temperature which permits binding of an exact match, but at which the mismatches with the original strand are sufficient to prevent binding. Plaques which hybridize with the probe are then picked, cultured, and the DNA recovered.

C.4. Verification of Construction For confirmation of vector construction, or for other sequencing, DNA is first amplified and isolated.
The isolated DNA is analyzed by restriction and/or sequenced by the dideoxy nucleotide method of Sanger, -19- ;~3~9~42 F., et al, Proc Natl Acad Sci (USA) (1977) 74:5463 as further described by Messing, et al, Nucleic Acids Res (1981) 9:309, or by the method of Maxam, et al, Methods in Enzymoloqy (1980) 65:499.
s ExamPles The following examples are intended to illustrate but not to limit the invention. In one ~~ aspect, the examples detail a method to retrieve the desi~ed cDNA sequences however, this process need not be repeated. The complete DNA sequence for coding region6 of the inserts in the PN-Ia and PN-IB clones are given in Figures 3 and 4, and standard synthetic methods may be used to construct either these precise sequences o~ the equivalent degenerate sequences employing alternate codons. Synthesis of DNA sequences of this length a~e by now nearly routine in the art.
See, for example, Edge et al, Nature (1981) 292: 756.
In addition, on 4 June 1986, ap~licants ha~e deposited at the ~merican Type Culture Collection, Rockville, Maryland, the PN-18 clone in phage ~gtlO having ATCC
No. 40238. This contains the relevant coding sequence for PN-Ia, which can be manipulated starting from the physical substance; the PN-I~ sequence can easily be obtained using site-specific mutagenesis.

ExamPle Purification of Native Protease Nexin-I
PN-I was prepared from serum-free conditioned medium, as described in Scott, R.W., et al. J Biol Chem (1985) (supra). Briefly, the harvested medium was filtered through a 45 ~ millipore*filter, and the proteins concent~ated by Amicon hollow fiber (*) Tcademark 1 ~ 3 ~ 2 filtration. The concentrated medium from a single 3 1 microcarrier culture was pas6ed over a 0.7 x 30 cm heparin-agarose column, preequilibrated in 0.3 M sodium chloride in phosphate buffer, and eluted with 1.0 M
sodium chloride in phosphate buffer, both containing 0.02% 60dium azide. Elution was obtained in 0.55-0.6 M
NaCl. The PN-I-containing fractions were concentrated by dialysi6 and then subjected to gel-exclusion chromatography by dialyzing 1-2 mg PN-I in 1 ml into column buffer containing 0.5 M NaCl, and applied to a 1 x 60 cm Bio-Gel* P-lOO(Bio-Rad 100-200 mesh) column and eluted with column buffer. The peak fractions were concentrated to 1 ml and stored at -80~C. The amino acid sequence and sugar composition were determined on this purified material.
The N-terminal amino acid sequence for the first 34 amino acids was determined with the results set forth above.

ExamPle 2 Isolation of Protease Nexin-I cDNA
Human foreskin fibroblasts were grown to confluence in 30 x 150 mm flask6, as described by Scott, R.W., J Biol Chem (1983) 258:10439, yielding approximately 1-2 x 10 cells. Twenty-four hr prior to harvest, cells were refed to stimulate the production of PN-I mRNA. The cells were harvested in the cold and washed twice with pho~phate buffered saline (PBS). The cell pellets were recovered, homogenized in buffer containing 20 mM vanadyl complex, and 0.2~ Nonidet*P-40 detergent, and then centrifuged for 10 min at 14,000 rpm. RNA was prepared from the supernatant using phenol/chloroform extraction and the total RNA obtained was subjected to oligo-dT affinity chromatography to obtain mRNA.

(*) Trademark 133964~

The isolated messenger was gel fractionated and probed with a mixture of twenty-four 14-mers having the sequence shown in Figure la, which represents the degenerate reverse complement of DNA encoding amino acids 20-24 of the determined N-terminal sequence. The probe hybridizes to mRNA of approximately 2500-2700 nucleotides in length.
The total mRNA preparation was then used as a template to preeare a cDNA library in ~gtlO, substantially as described by Huynh, T.V., et al, DNA
Cloninq Techniques: A Practical Approach (1984), Glover, D., ed, IRL, Oxford, but with second-strand synthe6is performed according to the method of Gubler, V., et al, Gene (1983) 25:263-269. The resulting cDNA was cut with ~5 EcoRI and inserted into the EcoRI site of ~gtlO, as described by Huynh et al (supra). Several million phage plaques were obtained and triplicate filter lifts were prepared. Plaques were duplicate screened under conditions of moderate stringency (6 x SSC at 30~C), with the 5' end P-ATP-labeled mixture of the 14-mers above. This resulted a number of positive clones.
Of the 60 clones pic~ed and cultured, 48 of them also hybridized under comparably stringent conditions to a 36-nucleotide oligomer of the sequence shown in Figure lb, which was a consensus sequence designed on the basis of amino acids 14-25, the sequence determined in the native protein.
Fifteen of these 48 clones were of approximately the size expected from the mRNA to be of sufficient length to encode the entire sequence. These fell into two classe6 by size: 2000 bp and 3000 bp. One 3000 bp clone was designated PN-18, and one 2000 bp clone was designated PN-33. These clones have similar coding sequences. Clones, designated PN-5, PN-8 and 13.3g6~

PN-ll have the same coding sequence as PN-18: clone PN-9 has the slightly different coding sequence included in PN-33. Restriction maps show these clones to include the 5' end of the gene: these maps are shown in Figure 2.
PN-18 was restricted with Sau3AI and cloned into the BamHI site of M13. To confirm the presence of the correct cDNA, the resulting M13 subclones were screened with the 14-mer mixture. Also, a 55 bp fragment was sequenced and found to contain the correct sequence encoding amino acids 17-34 of the native protein.
Thirteen of the above 15 clones contained a 750 bp EcoRI-BglII fragment which hybridizes to the 14-mer probe and is believed to encode the 5' portion of the gene. This segment has been sequenced, and the determined sequence includes the 55 bp Sau3AI fragment above, and the codons for the N-terminal sequence determined above, as well as codons for a putative 19 amino acid signal sequence extending back to an ATG.
The complete coding sequence for PN-Ia contained in PN-18 and the deduced amino acid sequence are shown in Figure 3. The first 19 encoded amino acids are a putative signal sequence, and the first 34 amino acids of the putative mature protein starting at the serine at position 20 correspond exactly to the N-terminus of the native protein. PN-18 is deposited with the American Type Culture Collection, and has accession number ATCC 40238.
Identification of PN-18 with PN-I production was verified by Northern blot, as shown in Figure 5.
The 55 bp Sau3AI fragment obtained from PN-18 was labeled and used to probe mRNA obtained from human foreskin fibroblasts and from several other cell lines not capable of PN-I production. The probe hybridizes 13~4~2 only to the mRNA of about 2.8 kb from the PN-I-producing cells.
The PN-33 clone which contains the DNA encoding PN-IB was also completely sequenced in the coding region 5 with the results shown, along with the deduced amino acid sequence, in Figure 4. As with PN-Ia, the first 19 encoded amino acids are a putative signal sequence, and the first 34 amino acids of the mature protein starting at the serine at position 20 correspond exactly 10 to the N-terminus of the native protein. The ~equence encoding PN-IB is almost identical to that of PN-Ia, except for the inclusion of an additional codon for glycine after that at position 310 of the mature protein and substitution of a threonine for an arginine residue 15 at that position. Thus, mature PN-Ia contains 378 amino acids; mature PN-IB contains 379.
The entire sequenced portions of PN-18 and PN-33 cDNA shown in Figures 3 and 4 are identical except for the codons corresponding to the above amino acid 20 sequence change. This was verified to be a difference in mRNA splicing by using PN-18 as a cDNA probe to retrieve a portion of the PN-I gene from a human genomic library. Sequencing in the region of the amino acid difference, which occurs between 2 adjacent exons 25 continuing into the introns separating them, established that there was a 3 bp difference in the splice site.
These results are shown in Figure 6. The A at the beginning of the codon at position 310 for arginine in PN-Ia is spliced 3 bp farther downstream into the next 30 exon than is the corresponding A in codon 310 for PN-IB.
Probes designed spanning this coding region which includes the foregoing Arg of PN-Ia and the Thr-Gly of PN-IB were used to estimate the relative 1~3~fi42 amounts of mRNA in human foreskin fibroblast preparations, and the relative amounts of cDNA in the corresponding cDNA libraries. The results of both of these Northern and Southern blots, respectively. showed that the two proteins are formed in approximately equal amounts. Thus, neither form appears to be "normal" or dominant.
The genomic DNA encoding the PN-I proteins was further studied as follows: Southern hybridization analysis of human DNA isolated from SK hepatoma cells was restricted with BglII, HindIII, or Eco RI.
Duplicate sample sets were fractionated on an agarose gel and electroblotted to a membrane filter. The resulting blots were hybridized to P labeled probes;
either the 2 kb PN insert (PN-33) or the 650 bp BglII
fragment from the 5' end. Based upon the pattern of hybridization obtained with the complete PN-I probes, the PN gene was estimated to span at least 20 kb. As expected, the 5' probe hybridized to a subset of the PN-I specific fragments and only a single band was seen for each enzyme digest. These results are consistent with a single PN-I gene.

ExamPle 3 Murine PN-I cDNA
In a manner similar to that described in Example 2, a cDNA library preeared in ~gtlO from mRNA
extracted from mouse fibroblasts is screened with the 55 bp Sau3AI fragment derived from PN-18. Phage hybridizing to this probe are then picked and cloned to obtain the desired murine PN-I cDNA.

-25- ~3~fi42 Example 4 Construction of ExPre~6ion Vectors The coding sequences from the EcoRI cas6ettes of PN-33 or PN-18 were each ligated into an amplifiable host expres6ion vector pSTH-MDH.

The amplifiable DHFR sequences are under control of the native promoter and followed by the termination 6equences of the hepatitis 6urface antigen gene. In the finished vector, the PN-I sequences are under control of the SV40 early promoter, and are also followed by hepatitis surface antigen termination sequences.
The DNAs encodng PN-Ia and PN-IB were inserted into the ho~t vector pSTH-MDH, in place of the tPA expression cassette, using three-way ligations in which the 5' and 3' ends of the coding sequences and appropriate portions of the expression systems were inserted as separate fragments. For the construction of these vectors, pSNaH-dhfr and pSNBH-dhfr, substantially equivalent ligations were performed, but with the appropriate starting materials.
For construction of pSNaH-dhfr, pNexa-HBV3'Rl, a vector containing the C-terminal-encoding portion of the gene followed by the hepatitis termination sequence~ was digested with BglII and EcoRI
and the 3' end of the expression sy6tem isolated. The vector pSV-Nexa, which contains the 5' end of the expression system, was digested with BglII and SalI and the vector portion containing the nexin 5' end isolated. These fragments were ligated with the DHFR
selectable marker, excised from pST~-MDH by EcoRI/SalI

1339fi42 digestion, in a three-way ligation and transformed into E. coli for selection and amplification. Plasmid DNA
representing the desired construction, pSNaH-dhfr, was isolated from the successful transformants.
In a precisely similar manner, pSN~H-dhfr was constructed, but using pNexB-HBV3lRI and pSV-NexB in place of the corresponding PN-Ia-containing vectors.
Common to these constructions is a vector containing the SV40 early promoter operably linked to the nexin 5' end which is common to both a and ~
forms. This intermediate vector, pSV-NexBalI, was constructed using PN-33, pUC18, and pSVoriHBV3'. PN-33 was cut with EcoRI to excise the PN-I-containing inserts, cut back with Bal31 and then digested with SacI
to obtain a tailored nexin insert containing the 5' end through the ATG start codon. This fragment was ligated into a HincII/SacI-digested pUC18 vector fragment to obtain pUCNex-BalI. pUCNex-BalI was cut with HindIII
and SalI to excise the nexin 5' end fragment common to the a and B forms which was then ligated into the HindIII/SalI-digested pSVori-HBV3l vector fragment (see below) to give the desired pSVNex-BalI.
An additional vector containing 3' sequences, pSVNex3~HBV, was constructed by digesting PN-33 with EcoRI and HpaI, isolating the 1650 bp fragment and ligating it into pUC18 digested with EcoRI and SmaI to obtain pUC-Nex3~. pUC-Nex3~ was supplied with hepatitis termination sequences by digesting with HindIII and BamHI and ligating the isolated nexin 3' end into HindIII/BamHI-digested pSVori-HV3' (see below) to obtain the desired pSVNex3~B V.
The two additional intermediate vectors, pS~Nexa and pSVNex~, were obtained using the 540 bp internal fragment from PN-33 or PN-18, as appropriate, 13~9fi42 and the corresponding 5~ and 3~ ends from pSVNex-BalI
and pSVNex3'HBV. In each case, pSVNex-BalI was digested with BqlII and SalI and pSVNex3~B V with HindIII and SalI and ligated in the three-way ligation with the BglII/HindIII 540 bp internal fragment of PN-Ia from PN-18 or PN-IB from PN-33 to obtain pSVNexa and pSVNex~, respectively. These were modified to place an EcoRI site at the extreme 3' end of the expression system by inserting the BglII/SacII insert of pSVNexa or pS~Nex~, as appropriate, into BamHI/SacII-digested pUC-HBV3'. The resulting vectors, pNexaHBV3'RI and pNexB B V3'RI, were then used in the constructions described above. The resulting vectors, generically named pSNH-dhfr, are diagrammed in Figure 7.
The vectors were transfected into COS-7 cells for transient expression, or into DHFR deficient CH0 cells, which were then amplified in methotrexate and cultured for the production of PN-Ia or PN-IB. The PN-I is secreted into the medium as the signal sequence is retained in the construct and is compatible with the host cells.
The media of the transformed cells are assayed for PN-I production using the thrombin binding assay described by Eaton, D.L., et al, J Cell Physiol (1983) 117:175-185. Briefly, serum-free medium preincubated with confluent cell cultures for 72 hr was centrifuged to remove cell debris. Labeled thrombin ( I-Th) at 0.1 ~g/ml was incubated with this medium for 45 min at 37~C. I-Th-PN complexes were resolved by SDS-polyacrylamide gel electrophoresis using 7% gels, under conditions which do not dissociate the Th-PN
complex, and quantitated in a gamma scintillation counter, assuming that PN and Th are present in equimolar amounts in Th-PN complexes. The complexes 1~3~642 formed are confirmed to contain PN-I by immunoprecipitation with PN-I rabbit antiserum.
The results of this assay show the production of PN-Ia or PN-I~ by appropriately transfected CH0 or COS7 cellG.

APPendix Construction of pSTH-MDH
pSVoriHBV3' contains the origin of replication and early and late promoters of SV40 upstream of the 3' termination sequences from the hepatitis B surface antigen gene with insertion sites for a foreign gene between them. pSVoriHBV3' is constructed from pML, SV40, and HBV. pML is digested with EcoRI, blunted with Klenow, and then digested with HindIII. The vector fragment containing the E. coli origin of replication and the ampicillin resistance gene is isolated and ligated to the isolated 540 bp fragment containing the early and late eromoters and origin of re~lication of SV40, obtained by digestion of SV40 DNA by HindIII and HinclI. The resulting vector, designated pSVori, is then digested with BamHI for acceptance of a 585 bp fragment isolated from a BamHI/BglII digest of HBV DNA
which contains the 3' termination sequences of the surface antigen gene. Correct orientation is confirmed by restriction analysis - digestion with HindIII and BamHI yields a 350 bp fragment from the correct vector.
The resulting ligated vector, pSVoriHBV3', thus contains the SV40 promoter and origin sequences upstream of the BV terminator and permits a coding sequence to be inserted conveniently between them.
Also prepared was ptPA-BAL17, which contains the tailored upstream portion of the tPA gene in a bacterial replication vector. The tPA cDNA is furnished 133~6i2 by the vector pMON-1068, which is a bacterial vector containing an insert of the entire cDNA sequence obtained for tPA ac described in Pennica, D. et al, Nature (1983) 30l:214-221. Of course, any bacterial replication vector containing this coding sequence could just as well have been used, and the restriction sites designated below fall within the disclosed sequence of the tPA cDNA set forth in the Nature reference.
pMON-1068 is first digested with BamHI to excise the tPA
encoding cDNA and then with BAL-31 to chew back at each end of the gene. Digestion with BAL-31 was continued until analysis of the lengths and sequence of linear fragments indicated that the 5' end of the fragment was within 17 bp of the ATG start codon. The precise distance of chew-back is not critical so long as it is within sufficiently short distance to permit the ATG to be placed an operable distance from the promoter in the expression cassette. A separation in this fragment of the 5' terminus from the ATG of about 10 bp is, in fact, 7referred. The selected linear fragment was then digested with SacI, which cuts inside the coding sequence of the tPA gene, and the resulting blunt/SacI
fragment was isolated. This contains the suitably tailored 5' end of the gene and was ligated into SacI/HincII-digested pUC13 to give the intermediate plasmid ptPA-BAL17.
pUC-DHFR was used as a cloning vector for the DHFR-encoding sequences, absent their associated control sequences. pUC-DHFR was constructed by digesting pDHFR-ll (Simonsen, C.C., et al, Proc Natl Acad Sci USA
(1983) 80:2495-2499) with Fnu4HI, blunting with Klenow and then digesting with BglII to isolate the 660 bp fragment as there described, and ligating this fragment into pUC13 which had been digested with HincII and 9fi~2 _30--BamHI. Thus, pUC-DHFR represents a straightforward cloning vector for DHFR analogous to the ptPA-BAL17 vector described for the 5' portion of the tPA gene above.
Finally, a separate cloning vector for the termination sequences derived from the hepatitis B
surface antigen gene, pUC-BV3', was constructed by digesting HBV DNA with BamHI and BglII and isolating the 585 bp fragment, as described above, and ligating this fragment into BamHI-digested pUC13.
pSV-tPA17, which contains the full-length tPA
coding sequence under control of SV40 promoter and HBV
terminating sequences was prepared as a three-way ligation of the vector fragment from pSVoriHBV3' digested with HindIII and BamHI, which thus provides the promoter and terminator along with vector sequences: the 3I portion of tPA obtained by SacI/BglII digestion of pMON-1068: and the tailored 5' portion of the tPA coding sequence, whic~ was obtained as a HindIII/SacI digest of ptPA-BAL17. The resulting ligation mixture was transfected into E. coli, the transformants selected for ampicillin resistance, and plasmid DNA containing the desired pSV-tPA~7 isolated.
The counterpart vector for DHFR expression, designated pSV-DHFR, was also obtained in a three-way ligation. Again the vector fragment obtained from HindIII/BamHI digestion of pSVoriHBV3' was used to provide the control sequences, and the 5l and 3' portions of the DHFR coding sequence were obtained by digestion of pUC-DHFR with HindIII and SacI (partial) and with BglII and TaqI (partial), respectively. The ligation mixture was used to transform E. coli, ampicillin resistant transformants were selected, and plasmid DNA, designated pSV-DHFR was isolated.

-31- i~ 42 A single plasmid containing a weak expression system for the DHFR coding se~uence was also prepared.
This plasmid, pMDH, was obtained in a 3-way ligation using the 1 kb fragment obtained by EcoRI/TaqI (partial) digestion of pDR34, the vector fragment from EcoRI/SalI-digested pML, and the 3' end of the gene isolated from SacI (partial)/SalI digested pSV-DHFR.
(The pDR34 vector i8 described by Gasser, C.S., et al, Proc Natl Acad Sci USA (1982) 79:65Z2-6526, supra) and contains the mouse DHFR gene linked to its own promoter.) The resulting vector, pMDH, is analogous to pSV-DHFR, except that the DHFR gene is under control of the murine DHFR promoter. The weak expression cassette residing on pMDH and strong expression cassette residing on pSV-tPA17, when used in admixture to transfect suitable DHFR-deficient cells, thus constitute one embodiment of the expression system of the invention.
Finally, pSTH-MDH, which contains the expression cassettes for tPA and for DHFR on a single vector, was constructed as a three-way ligation of the appropriate isolated fragments of pSV-tPA17, pMDH, and pUC-B V3'. pSV-tPA17 is digested with SacII and SalI, pMDH with EcoRI and SmaI, and pUC-HBV3' with SacII and EcoRI.

Claims (7)

1. A method to purify protease nexin 1 (PN-1), which method comprises:
applying a medium containing PN-I to a column containing heparin bound to solid support, said column being preequilibrated, eluting said column with a gradient of 0.3-1M NaCl to obtain fractions, recovering the fractions containing classes of PN-I, followed by subjecting said fractions to gel exclusion chromalography using a gel with an exclusion of 100 kd.

2. The method of claim 1 wherein the heparin is bound to agarose support.

3. The method of claim 1 wherein the PN-I containing medium is serum-free medium conditioned by human foreskin fibroblasts.

4. The method of claim 3 wherein the fibroblasts are grown in microcarrier culture.

5. The method of claim 1 wherein the column is preequilibrated with a solution comprising 0.3M NaCl.

6. The method of claim 1 wherein the protease nexin-I is native protease nexin-I.

7. The method of claim 1 wherein the protease nexin-I is recombinant protease nexin-I.