可药性
脂质双层融合
计算生物学
化学
小分子
融合
病毒包膜
细胞生物学
药物发现
包络线(雷达)
生物
膜
病毒学
融合蛋白
药物靶点
内膜
生物物理学
纳特
穗蛋白
作者
F. Javier Luque,Marı́a-José Camarasa
出处
期刊:ChemMedChem
[Wiley]
日期:2020-07-28
卷期号:16 (1): 105-107
被引量:5
标识
DOI:10.1002/cmdc.202000411
摘要
Abstract Here we highlight a sound and unique work reported by Chen and co‐workers entitled “HIV‐1 fusion inhibitors targeting the membrane‐proximal external region of Env spikes” (Xiao et al., Nat. Chem. Biol . 2020 , 16 , 529). In this article, the authors identify, by means of a clever antibody‐guided strategy, several small molecules as fusion inhibitors of HIV‐1 replication acting at the membrane proximal external region (MPER) of the HIV‐1 envelope (Env) spike. MPER, which was previously recognized as a vaccine target, emerges as a novel druggable target for the discovery of HIV‐1 fusion inhibitors. The compounds (exemplified by dequalinium and dequalinium‐inspired analogues) prevent the conformational changes of Env from the prefusion species to the intermediate states required for membrane fusion. This work not only paves the way to novel, specific and useful anti‐HIV‐1 inhibitors, but also discloses new therapeutic strategies against other infectious diseases.
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