Interactions between the N-terminal tail and the gating machinery of hERG K+ channels both in closed and open/inactive states

被引:11
|
作者
de la Pena, Pilar [1 ]
Machin, Angeles [1 ]
Fernandez-Trillo, Jorge [1 ]
Dominguez, Pedro [1 ]
Barros, Francisco [1 ]
机构
[1] Univ Oviedo, Dept Biochem & Mol Biol, E-33006 Oviedo, Spain
来源
关键词
Potassium channel; Ether-a-go-go-related gene; Disulfide bridging; Structure-function relationship; Cytoplasmic domains; Gating modulation; ACTIVATED HCN CHANNELS; DOMAIN; PROXIMITY; CYSTEINE; LINKER; REGION;
D O I
10.1007/s00424-014-1612-1
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The N-terminal-most N-tail of the human ether-A -go-go-related gene (hERG) potassium channel is a crucial modulator of deactivation through its interactions with the S4-S5 loop and/or the C-linker/cNBD, leading to a stabilization of the channel's open state. Not only the N-terminal, but also the initial C-terminal region of the channel can modulate the transitions between the open and closed states either by direct or by indirect/allosteric interactions with the gating machinery. However, while a physical proximity of the N-tail to the gating machinery has been demonstrated in the closed state, data about their possible interaction in other channel conformations have been lacking. Using a site-directed cysteine mutagenesis and disulfide chemistry approach, we present here evidence that a physical proximity between the N-tail and the gating-related structures can also exist in channels held between pulses in the open/inactive state, highlighting the physiological and functional relevance of the direct interactions between the N-terminal tail and the S4-S5 loop and/or C-linker structures for modulation of channel.
引用
收藏
页码:1747 / 1756
页数:10
相关论文
共 44 条