Antigenicity-defined conformations of an extremely neutralization-resistant HIV-1 envelope spike
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Author
Cai, Yongfei
Karaca-Griffin, Selen
Chen, Jia
Tian, Sai
Fredette, Nicholas
Linton, Christine
Rits-Volloch, Sophia
Lu, Jianming
Wagh, Kshitij
Theiler, James
Korber, Bette
Seaman, Michael
Harrison, Stephen
Carfi, Andrea
Chen, Bing
Published Version
https://doi.org/10.1073/pnas.1700634114Metadata
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Cai, Yongfei, Selen Karaca-Griffin, Jia Chen, Sai Tian, Nicholas Fredette, Christine E. Linton, Sophia Rits-Volloch, et al. 2017. “Antigenicity-Defined Conformations of an Extremely Neutralization-Resistant HIV-1 Envelope Spike.” Proceedings of the National Academy of Sciences 114 (17): 4477–82. doi:10.1073/pnas.1700634114.Abstract
The extraordinary genetic diversity of the HIV-1 envelope spike [Env; trimeric (gp160)(3), cleaved to (gp120/gp41)(3)] poses challenges for vaccine development. Envs of different clinical isolates exhibit different sensitivities to antibody-mediated neutralization. Envs of difficult-to-neutralize viruses are thought to be more stable and conformationally homogeneous trimers than those of easy-to-neutralize viruses, thereby providing more effective concealment of conserved, functionally critical sites. In this study we have characterized the antigenic properties of an Env derived from one of the most neutralization-resistant HIV-1 isolates, CH120.6. Sequence variation at neutralizing epitopes does not fully account for its exceptional resistance to antibodies. The full-length, membrane-bound CH120.6 Env is indeed stable and conformationally homogeneous. Its antigenicity correlates closely with its neutralization sensitivity, and major changes in antigenicity upon CD4 engagement appear to be restricted to the coreceptor site. The CH120.6 gp140 trimer, the soluble and uncleaved ectodomain of (gp160)(3), retains many antigenic properties of the intact Env, consistent with a conformation close to that of Env spikes on a virion, whereas its monomeric gp120 exposes many nonneutralizing or strain-specific epitopes. Thus, trimer organization and stability are important determinants not only for occluding many epitopes but also for conferring resistance to neutralization by all but a small set of antibodies. Env preparations derived from neutralization-resistant viruses may induce irrelevant antibody responses less frequently than do other Envs and may be excellent templates for developing soluble immunogens.Terms of Use
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