毛有东
Professor

Gender:Male

Date of Birth:1977-04-06

Alma Mater:Peking University

Education Level:Postgraduate (Doctoral)

[MORE] Academic Honor:

2021  Winner of National Science Fund for Distinguished Young Scholars

Honors and Titles:

北京大学黄廷方/信和青年杰出学者奖

博雅青年学者奖

MOBILE Version

Paper Publications

Asymmetric Structures and Conformational Plasticity of the Uncleaved Full-Length Human Immunodeficiency Virus Envelope Glycoprotein Trimer

Release time:2022-06-24 Hits:

Impact Factor:5.0

DOI number:10.1128/JVI.00529-21

Journal:J. Virol.

Abstract:The functional human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimer [(gp120/gp41)3] is produced by cleavage of a conformationally flexible gp160 precursor. gp160 cleavage or the binding of BMS-806, an entry inhibitor, stabilizes the pretriggered, "closed" (state 1) conformation recognized by rarely elicited broadly neutralizing antibodies. Poorly neutralizing antibodies (pNAbs) elicited at high titers during natural infection recognize more "open" Env conformations (states 2 and 3) induced by binding the receptor, CD4. We found that BMS-806 treatment and cross-linking decreased the exposure of pNAb epitopes on cell surface gp160; however, after detergent solubilization, cross-linked and BMS-806-treated gp160 sampled non-state-1 conformations that could be recognized by pNAbs. Cryo-electron microscopy of the purified BMS-806-bound gp160 revealed two hitherto unknown asymmetric trimer conformations, providing insights into the allosteric coupling between trimer opening and structural variation in the gp41 HR1N region. The individual protomer structures in the asymmetric gp160 trimers resemble those of other genetically modified or antibody-bound cleaved HIV-1 Env trimers, which have been suggested to assume state-2-like conformations. Asymmetry of the uncleaved Env potentially exposes surfaces of the trimer to pNAbs. To evaluate the effect of stabilizing a state-1-like conformation of the membrane Env precursor, we treated cells expressing wild-type HIV-1 Env with BMS-806. BMS-806 treatment decreased both gp160 cleavage and the addition of complex glycans, implying that gp160 conformational flexibility contributes to the efficiency of these processes. Selective pressure to maintain flexibility in the precursor of functional Env allows the uncleaved Env to sample asymmetric conformations that potentially skew host antibody responses toward pNAbs.

Indexed by:Journal paper

Discipline:Natural Science

Document Type:J

Volume:95

Issue:24

Page Number:e0052921

Translation or Not:no

Date of Publication:2021-11-23

Included Journals:SCI

First Author:Shijian Zhang,Kunyu Wang

Correspondence Author:Joseph Sodroski,Youdong Mao

All the Authors:Wei Li Wang,Hanh T Nguyen,Shuobing Chen,Maolin Lu,Eden P Go,Haitao Ding,Robert T Steinbock,Heather Desaire

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