Binding of the third variable region (V3) of the HIV-1 envelope glycoprotein gp120 to the cell-surface coreceptors CCR5 or CXCR4 during viral entry suggests that there are conserved structural elements in this sequence-variable region. These conserved elements could serve as epitopes to be targeted by a vaccine against HIV-1. Here we perform a systematic structural analysis of representative human anti-V3 monoclonal antibodies in complex with V3 peptides, revealing that the crown of V3 has four conserved structural elements: an arch, a band, a hydrophobic core and the peptide backbone. These are either unaffected by or are subject to minimal sequence variation. As these regions are targeted by cross-clade neutralizing human antibodies, they provide a blueprint for the design of vaccine immunogens that could elicit broadly cross-reactive protective antibodies. © 2010 Nature America, Inc. All rights reserved.
CITATION STYLE
Jiang, X., Burke, V., Totrov, M., Williams, C., Cardozo, T., Gorny, M. K., … Kong, X. P. (2010). Conserved structural elements in the V3 crown of HIV-1 gp120. Nature Structural and Molecular Biology, 17(8), 955–961. https://doi.org/10.1038/nsmb.1861
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