PubMed 11339975
Referenced in: none
Automatically associated channels: Kv11.1
Title: HERG K+ channels: friend and foe.
Authors: J I Vandenberg, B D Walker, T J Campbell
Journal, date & volume: Trends Pharmacol. Sci., 2001 May , 22, 240-6
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/11339975
Abstract
The K+ channel encoded by the human ether-à-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.