Structural basis for K(V)7.1-KCNE(x) interactions in the I(Ks) channel complex.
Structural basis for K(V)7.1-KCNE(x) interactions in the I(Ks) channel complex.
复制标题
DOI:
10.1016/j.hrthm.2009.12.017
复制
发表时间:
2010-05
期刊:
影响因子:
5.5
通讯作者:
Schmitt, Nicole
中科院分区:
文献类型:
--
作者:
Lundby, Alicia;Tseng, Gea-Ny;Schmitt, Nicole
The cardiac IKs current is involved in action potential repolarization, where its primary function is to limit action potential prolongation during sympathetic stimulation. The IKs channel is mainly composed of KV7.1 ion channels associated with KCNE1 auxiliary subunits. The availability of KCNE1 solution structure by nuclear magnetic resonance spectroscopy in conjunction with biochemical assays addressing KV7.1–KCNE1 residue interactions has provided new insights into the structural basis for KV7.1 modulation by KCNE1. Recent evidence further suggests that KCNE2 may associate with the KV7.1–KCNE1 channel complex and modulate its current amplitude. Here we review recent studies in this area and discuss potential roles for multiple KCNEx subunits in IKs generation and modulation as well as the clinical relevance of the new information.
登录
查看更多内容
影响因子:
5.5
作者:
Gaborit, Nathalie;Le Bouter, Sabrina;Demolombe, Sophie
通讯作者:
Demolombe, Sophie
影响因子:
10.8
作者:
Chouabe, C;Neyroud, N;Barhanin, J
通讯作者:
Barhanin, J
影响因子:
4.8
作者:
Franqueza, L;Lin, M;Sanguinetti, MC
通讯作者:
Sanguinetti, MC
影响因子:
8.4
作者:
Delpon, Eva;Cordeiro, Jonathan M.;Antzelevitch, Charles
通讯作者:
Antzelevitch, Charles
影响因子:
56.9
作者:
de Lichtenberg, U;Jensen, LJ;Bork, P
通讯作者:
Bork, P