| Literature DB >> 16284180 |
Chih-chin Huang1, Min Tang, Mei-Yun Zhang, Shahzad Majeed, Elizabeth Montabana, Robyn L Stanfield, Dimiter S Dimitrov, Bette Korber, Joseph Sodroski, Ian A Wilson, Richard Wyatt, Peter D Kwong.
Abstract
The third variable region (V3) of the HIV-1 gp120 envelope glycoprotein is immunodominant and contains features essential for coreceptor binding. We determined the structure of V3 in the context of an HIV-1 gp120 core complexed to the CD4 receptor and to the X5 antibody at 3.5 angstrom resolution. Binding of gp120 to cell-surface CD4 would position V3 so that its coreceptor-binding tip protrudes 30 angstroms from the core toward the target cell membrane. The extended nature and antibody accessibility of V3 explain its immunodominance. Together, the results provide a structural rationale for the role of V3 in HIV entry and neutralization.Entities:
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Year: 2005 PMID: 16284180 PMCID: PMC2408531 DOI: 10.1126/science.1118398
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728