脂质双层融合
病毒进入
病毒包膜
趋化因子受体
趋化因子受体CCR5
合理设计
生物
细胞融合
糖蛋白
受体
细胞生物学
CXCR4型
人类免疫缺陷病毒(HIV)
病毒学
进入抑制剂
CCR5受体拮抗剂
恩夫韦肽
疱疹病毒糖蛋白B
第41页
病毒复制
病毒
细胞
趋化因子
免疫学
生物化学
遗传学
抗体
表位
作者
Tianshu Xiao,Yongfei Cai,Bing Chen
出处
期刊:Viruses
[MDPI AG]
日期:2021-04-23
卷期号:13 (5): 735-735
被引量:31
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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