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filingDate 1991-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34094bcf3d8fea3212adea3532f6c3a0
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publicationDate 2002-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0551440-B1
titleOfInvention Design of bioactive peptides based on immunoglobulin structure
abstract The present invention relates to a method for producing peptides which have biological activity comprising: (i) identifying a region of a protein of interest which is homologous to a member of the immunoglobulin superfamily of molecules; (ii) synthesizing a peptide which comprises amino acid sequence found in the region of homology; and (iii) modifying the synthetic peptide such that it assumes a three-dimensional conformation which is biologically active. The invention is based, in part, on the discovery that a cyclic peptide comprising amino acid sequences of a CDR derived from an antibody directed toward a viral receptor molecule can be used to effectively inhibit the binding of virus to its receptor. The invention is also based in part on the discovery that a cyclic peptide corresponding to a portion of human immunodeficiency virus (HIV) gp120 that is homologous to immunoglobulins may be used to generate an anti-HIV immune response.
priorityDate 1990-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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