赫尔格
钾通道
心脏动作电位
复极
长QT综合征
生物
钾通道阻滞剂
离子通道
生物物理学
电生理学
药理学
QT间期
生物化学
内科学
神经科学
受体
医学
作者
Weiwei Wang,Roderick MacKinnon
出处
期刊:Cell
[Cell Press]
日期:2017-04-01
卷期号:169 (3): 422-430.e10
被引量:433
标识
DOI:10.1016/j.cell.2017.03.048
摘要
The human ether-à-go-go-related potassium channel (hERG, Kv11.1) is a voltage-dependent channel known for its role in repolarizing the cardiac action potential. hERG alteration by mutation or pharmacological inhibition produces Long QT syndrome and the lethal cardiac arrhythmia torsade de pointes. We have determined the molecular structure of hERG to 3.8 Å using cryo-electron microscopy. In this structure, the voltage sensors adopt a depolarized conformation, and the pore is open. The central cavity has an atypically small central volume surrounded by four deep hydrophobic pockets, which may explain hERG’s unusual sensitivity to many drugs. A subtle structural feature of the hERG selectivity filter might correlate with its fast inactivation rate, which is key to hERG’s role in cardiac action potential repolarization.
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