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filingDate 1991-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34094bcf3d8fea3212adea3532f6c3a0
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publicationDate 1993-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0551440-A1
titleOfInvention Design of bioactive peptides based on immunoglobulin structure
abstract This invention relates to a method for producing peptides which have biological activity, said method comprising the following steps: (i) identifying a region of a protein to be studied which is homologous to a member of the molecule superfamily immunoglobulin; (ii) synthesizing a peptide which has an amino acid sequence found in the region of homology; and (iii) modifying the synthetic peptide so that it adopts a three-dimensional conformation which is biologically active. This invention is based, on the one hand, on the discovery that a cyclic peptide comprising amino acid sequences of a complementary determination region from an antibody against a viral receptor molecule can be used to inhibit effective fixation of the virus on its receptor. The invention is also based in part on the discovery that a cyclic peptide corresponding to a part of the human immunodeficiency virus (HIV) gp120 which is homologous to immunoglobulins can be used to produce an anti-HIV immune response.
priorityDate 1990-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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