第41页
糖蛋白
小分子
进入抑制剂
化学
人类免疫缺陷病毒(HIV)
对接(动物)
病毒进入
细胞生物学
跨膜蛋白
病毒
生物
生物化学
病毒学
抗原
医学
免疫学
病毒复制
受体
护理部
表位
出处
期刊:Springer eBooks
[Springer Nature]
日期:2022-01-01
卷期号:: 27-43
标识
DOI:10.1007/978-981-16-8702-0_3
摘要
Interrupting early events in the virus life cycle, such as those prior to the formation of provirus, could effectively prevent HIV-1 infection. HIV-1 entry into host cells is mediated by the envelope glycoprotein (Env) trimer, which is composed of three gp120 exterior glycoproteins and three gp41 transmembrane glycoproteins. Hence, the development of novel inhibitors targeting these two glycoproteins could hold the key to early inhibition of HIV-1 infection. Small-molecule entry inhibitors targeting early events in the virus life cycle comprise a well-established class of useful drugs. Many libraries of small-molecule inhibitors have been established to screen potential drug candidates for a variety of targets based on computer docking, FRET, or peptide-linked assay. This chapter reviews the mechanisms of some small-molecule inhibitors targeting HIV-1 gp120 and gp41 and corresponding high-efficiency screening strategies for potential small-molecule inhibitors.
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