HERG K+ channels: friend and foe

被引:221
作者
Vandenberg, JI
Walker, BD
Campbell, TJ
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] St Vincents Hosp, Victor Chang Cardiac Res Inst, Sydney, NSW 2010, Australia
[3] St Vincents Hosp, Ctr Immunol, Sydney, NSW 2010, Australia
[4] Univ New S Wales, Dept Med, Sydney, NSW 2010, Australia
关键词
D O I
10.1016/S0165-6147(00)01662-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The K+ channel encoded by the human ether-a-go-go related gene (HERG) is one of many ion channels that are crucial for normal action potential repolarization in cardiac myocytes, HERG encodes the pore-forming subunit of the rapid component of the delayed rectifier K+ channel, I-K(Vr). HERG K+ channels are of considerable pharmaceutical interest as possible therapeutic targets for anti-arrhythmic agents and as the molecular target responsible for the cardiac toxicity of a wide range of pharmaceutical agents. Recent studies of the molecular basis of the promiscuity of HERG K+ channel drug binding has not only started to shed light on this tricky pharmaceutical problem but has also provided further insights into the structure and function of HERG K+ channels.
引用
收藏
页码:240 / 246
页数:7
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