HIV-1 Entry and Membrane Fusion Inhibitors

被引:51
|
作者
Xiao, Tianshu [1 ,2 ]
Cai, Yongfei [1 ,2 ]
Chen, Bing [1 ,2 ]
机构
[1] Boston Childrens Hosp, Div Mol Med, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Pediat, Blackfan St, Boston, MA 02115 USA
来源
VIRUSES-BASEL | 2021年 / 13卷 / 05期
关键词
HIV; envelope glycoprotein; viral entry; membrane fusion; fusion inhibitor; IMMUNODEFICIENCY-VIRUS TYPE-1; CRYO-EM STRUCTURE; GP120 ENVELOPE GLYCOPROTEIN; SMALL-MOLECULE INHIBITOR; CRYSTAL-STRUCTURE; CHEMOKINE RECEPTORS; STRUCTURAL BASIS; PHENOTYPIC RESISTANCE; ATTACHMENT INHIBITOR; CYTOPLASMIC DOMAIN;
D O I
10.3390/v13050735
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HIV-1 (human immunodeficiency virus type 1) infection begins with the attachment of the virion to a host cell by its envelope glycoprotein (Env), which subsequently induces fusion of viral and cell membranes to allow viral entry. Upon binding to primary receptor CD4 and coreceptor (e.g., chemokine receptor CCR5 or CXCR4), Env undergoes large conformational changes and unleashes its fusogenic potential to drive the membrane fusion. The structural biology of HIV-1 Env and its complexes with the cellular receptors not only has advanced our knowledge of the molecular mechanism of how HIV-1 enters the host cells but also provided a structural basis for the rational design of fusion inhibitors as potential antiviral therapeutics. In this review, we summarize our latest understanding of the HIV-1 membrane fusion process and discuss related therapeutic strategies to block viral entry.
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页数:19
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