Abstract
We have determined the crystal structure of the broadly neutralizing antibody (bnAb) AP33, bound to a peptide corresponding to hepatitis C virus (HCV) E2 envelope glycoprotein antigenic site 412 to 423. Comparison with bnAb HCV1 bound to the same epitope reveals a different angle of approach to the antigen by bnAb AP33 and slight variation in its β-hairpin conformation of the epitope. These structures establish two different modes of binding to E2 that antibodies adopt to neutralize diverse HCV.
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Antibodies, Neutralizing / chemistry*
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Antibodies, Neutralizing / metabolism
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Epitopes / chemistry
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Epitopes / genetics
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Hepacivirus / genetics*
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Models, Molecular*
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Protein Conformation*
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Viral Envelope Proteins / chemistry*
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Viral Envelope Proteins / genetics
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Viral Envelope Proteins / metabolism
Substances
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Antibodies, Neutralizing
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Epitopes
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Viral Envelope Proteins
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glycoprotein E2, Hepatitis C virus