GB1058828A - Process for the manufacture of artificial antigens - Google Patents
Process for the manufacture of artificial antigensInfo
- Publication number
- GB1058828A GB1058828A GB3885563A GB3885563A GB1058828A GB 1058828 A GB1058828 A GB 1058828A GB 3885563 A GB3885563 A GB 3885563A GB 3885563 A GB3885563 A GB 3885563A GB 1058828 A GB1058828 A GB 1058828A
- Authority
- GB
- United Kingdom
- Prior art keywords
- protein
- diisocyanate
- linking
- albumin
- component
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/006—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length of peptides containing derivatised side chain amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/107—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
- C07K1/1072—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
- C07K1/1075—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups by covalent attachment of amino acids or peptide residues
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Peptides Or Proteins (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Abstract
Artificial antigens are produced by linking a carrier protein via an organic bridge group to a serologically determinant peptide, e.g. a protein hormone, toxin, enzyme or a virus or bacterium having a surface component with protein characteristics. The linkage may be formed by a chemical process such as forming a diazo or azide derivative of one component which is coupled to the phenolic hydroxyl or amine groups of the other or by cross-linking the two components by reaction with a diisocyanate. The specific example relates to a product obtained by formation of a diazo group-containing derivative of a C-terminal hexapeptide obtained by enzymatic digestion of tobacco mosaic virus and coupling with a diisocyanate-cross -linked cattle albumin. Suitable carrier proteins are egg albumin, serum albumin, lactalbumin, g -globulins and gelatin and its derivatives.ALSO:Artificial antigens are produced by linking a "carrier protein" via an organic bridge group to a serologically determinant peptide. Suitable carrier proteins are: egg albumin, lacta bumin, serum albumin, g -globulins and gelatin and its derivatives. The serologically determinant peptide may be a protein hormone, toxin, enzyme or a virus or bacterium whose surface component has protein characteristics. The linkage may be formed by a chemical process such as (1) forming a diazo derivative of one component, which is coupled to a phenolic hydroxyl group of the other, (2) by similarly forming an azide of one component, which is coupled to the amino group of the other or (3) by cross-linking the two components by reaction with a diisocyanate. The specific example relates to a product obtained by formation of a diazo derivative of a C-terminal hexapeptide obtained by enzymatic digestion of the tobacco mosaic virus and coupling with a diisocyanate cross-linked cattle albumin.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB0072720 | 1963-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1058828A true GB1058828A (en) | 1967-02-15 |
Family
ID=6977565
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3885563A Expired GB1058828A (en) | 1963-07-17 | 1963-10-02 | Process for the manufacture of artificial antigens |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1467782A1 (en) |
GB (1) | GB1058828A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2421943A1 (en) * | 1973-05-07 | 1974-11-28 | Univ Ohio | MODIFIED POLYPEPTIDES |
DE2646223A1 (en) * | 1975-10-14 | 1977-04-28 | Univ Ohio | NEW IMPROVED ORGANIC COMPOUNDS |
EP0094844A2 (en) * | 1982-05-18 | 1983-11-23 | The Regents Of The University Of California | Drug-carrier conjugates |
EP0095426A1 (en) * | 1982-05-26 | 1983-11-30 | CNRS, Centre National de la Recherche Scientifique | Synthetic polypeptides containing at least one sequence of the choleric B1 sub-unit toxin, and medicines containing them |
FR2532850A1 (en) * | 1982-09-15 | 1984-03-16 | Pasteur Institut | Immunogenic conjugates between a hapten and a carrier molecule derived from a toxin, vaccines comprising them and method for obtaining them |
US6146633A (en) * | 1973-05-07 | 2000-11-14 | The Ohio State University | Method for treatment of antigenically modified polypeptides |
CN104383889A (en) * | 2014-11-21 | 2015-03-04 | 中国农业科学院油料作物研究所 | Dihydrocapsaicin polyclonal antibody immunoadsorbent, immunoaffinity column and preparation method and application thereof |
CN104447383A (en) * | 2014-11-21 | 2015-03-25 | 中国农业科学院油料作物研究所 | Dihydrocapsaicin artificial hapten and artificial antigen as well as preparation methods thereof |
-
1963
- 1963-07-17 DE DE19631467782 patent/DE1467782A1/en active Pending
- 1963-10-02 GB GB3885563A patent/GB1058828A/en not_active Expired
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2421943A1 (en) * | 1973-05-07 | 1974-11-28 | Univ Ohio | MODIFIED POLYPEPTIDES |
US6146633A (en) * | 1973-05-07 | 2000-11-14 | The Ohio State University | Method for treatment of antigenically modified polypeptides |
DE2646223A1 (en) * | 1975-10-14 | 1977-04-28 | Univ Ohio | NEW IMPROVED ORGANIC COMPOUNDS |
EP0094844A3 (en) * | 1982-05-18 | 1984-11-21 | The Regents Of The University Of California | Drug-carrier conjugates |
EP0094844A2 (en) * | 1982-05-18 | 1983-11-23 | The Regents Of The University Of California | Drug-carrier conjugates |
US4587046A (en) * | 1982-05-18 | 1986-05-06 | The Regents Of The University Of California | Drug-carrier conjugates |
EP0095426A1 (en) * | 1982-05-26 | 1983-11-30 | CNRS, Centre National de la Recherche Scientifique | Synthetic polypeptides containing at least one sequence of the choleric B1 sub-unit toxin, and medicines containing them |
FR2527445A1 (en) * | 1982-05-26 | 1983-12-02 | Centre Nat Rech Scient | MEDICINAL PRODUCTS CONTAINING AT LEAST ONE SEQUENCE OF THE CHOLERIC TOXIN B1 SUBUNIT |
FR2532850A1 (en) * | 1982-09-15 | 1984-03-16 | Pasteur Institut | Immunogenic conjugates between a hapten and a carrier molecule derived from a toxin, vaccines comprising them and method for obtaining them |
CN104383889A (en) * | 2014-11-21 | 2015-03-04 | 中国农业科学院油料作物研究所 | Dihydrocapsaicin polyclonal antibody immunoadsorbent, immunoaffinity column and preparation method and application thereof |
CN104447383A (en) * | 2014-11-21 | 2015-03-25 | 中国农业科学院油料作物研究所 | Dihydrocapsaicin artificial hapten and artificial antigen as well as preparation methods thereof |
CN104447383B (en) * | 2014-11-21 | 2016-03-23 | 中国农业科学院油料作物研究所 | A kind of Dihydrocapsaicin artificial semiantigen, artificial antigen and preparation method thereof |
CN104383889B (en) * | 2014-11-21 | 2016-08-24 | 中国农业科学院油料作物研究所 | A kind of Dihydrocapsaicin polyclonal antibody adsorbent, immune affinity column and its preparation method and application |
Also Published As
Publication number | Publication date |
---|---|
DE1467782A1 (en) | 1968-12-12 |
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