第41页
脂质双层融合
生物
病毒进入
病毒包膜
趋化因子受体
糖蛋白
细胞生物学
疱疹病毒糖蛋白B
趋化因子受体CCR5
受体
细胞融合
人类免疫缺陷病毒(HIV)
病毒学
计算生物学
病毒复制
趋化因子
细胞
病毒
免疫学
生物化学
抗体
表位
标识
DOI:10.1016/j.tim.2019.06.002
摘要
HIV-1 envelope glycoprotein [Env; trimeric (gp160)3 cleaved to (gp120/gp41)3] attaches the virion to a susceptible cell and induces fusion of viral and cell membranes to initiate infection. It interacts with the primary receptor CD4 and coreceptor (e.g., chemokine receptor CCR5 or CXCR4) to allow viral entry by triggering large structural rearrangements and unleashing the fusogenic potential of gp41 to induce membrane fusion. Recent advances in structural biology of HIV-1 Env and its complexes with the cellular receptors have revealed molecular details of HIV-1 entry and yielded new mechanistic insights. In this review, I summarize our latest understanding of the HIV-1 membrane fusion process and discuss possible pathways for productive viral entry.
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