Antigenic peptides containing large PEG loops designed to extend but of the HLA-A2 binding site form stable complexes with class I major histocompatibility complex molecules

Proceedings of the National Academy of Sciences of the United States of America

Volumn 93, Issue 10, 1996, Pages 4583-4588

  Bouvier, Marlène ^a   Wiley, Don C ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1;

ANTIGENICITY; ARTICLE; BINDING AFFINITY; BINDING SITE; CIRCULAR DICHROISM; HLA SYSTEM; IMMUNE RESPONSE; IMMUNE SYSTEM; MAJOR HISTOCOMPATIBILITY COMPLEX; PRIORITY JOURNAL; PROTEIN ANALYSIS; T LYMPHOCYTE ACTIVATION;

AMINO ACID SEQUENCE; ANTIGENS; BINDING SITES; DRUG DESIGN; DRUG STABILITY; GENE PRODUCTS, TAX; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA-A2 ANTIGEN; HUMANS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; PEPTIDES, CYCLIC; POLYETHYLENE GLYCOLS; PROTEIN CONFORMATION; PROTEIN FOLDING; RECOMBINANT PROTEINS; SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT;

EID: 0029897206     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.10.4583     Document Type: Article

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