Volume 9 Supplement 2
Structural basis for germline gene usage of a potent class of antibodies targeting the CD4 binding site of HIV-1 gp120
© West et al; licensee BioMed Central Ltd. 2012
Published: 13 September 2012
A large number of anti-HIV-1 antibodies targeting the CD4 binding site (CD4bs) on gp120 have recently been reported. These antibodies, typified by VRC01, are remarkable for both their breadth and potency. Crystal structures have revealed a common mode of binding for several of these antibodies; however, the precise relationship among CD4bs antibodies remains to be defined.
We analyze existing structural and sequence data, propose a set of signature features for potent VRC01-like (PVL) antibodies, and test the importance of these features by mutagenesis.
A group of highly potent CD4bs antibodies, previously isolated from 5 different individuals, all derive from the human VH1-2 gene segment and share a set of characteristic residues, including W50, N58, R71, and W100B. Mutagenesis studies on a half-germline version of a VRC01-like antibody confirm that these signature residues are critical for gp120 binding. Neutralization assays with viruses mutated at sites that contact these critical antibody residues also confirm the significance of these interactions.
The signature features explain why PVL antibodies derive from a single germ-line human VH gene segment and why certain gp120 sequences are associated with antibody resistance. This analysis also suggests that immunization experiments to elicit VRC01-like antibodies may be problematic in mice or rabbits since they lack germ-line VH genes with all the critical residues. Our results bear on vaccine development and structure-based design to improve the potency and breadth of anti-CD4bs antibodies.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.