A unique mechanism of inactivation gating of the Kv channel family member Kv7.1 and its modulation by PIP2 and calmodulin

Kv通道家族成员Kv7.1独特的失活门控机制及其受PIP2和钙调蛋白的调节

阅读:1

Abstract

Inactivation of voltage-gated K(+) (Kv) channels mostly occurs by fast N-type or/and slow C-type mechanisms. Here, we characterized a unique mechanism of inactivation gating comprising two inactivation states in a member of the Kv channel superfamily, Kv7.1. Removal of external Ca(2+) in wild-type Kv7.1 channels produced a large, voltage-dependent inactivation, which differed from N- or C-type mechanisms. Glu(295) and Asp(317) located, respectively, in the turret and pore entrance are involved in Ca(2+) coordination, allowing Asp(317) to form H-bonding with the pore helix Trp(304), which stabilizes the selectivity filter and prevents inactivation. Phosphatidylinositol 4,5-bisphosphate (PIP2) and Ca(2+)-calmodulin prevented Kv7.1 inactivation triggered by Ca(2+)-free external solutions, where Ser(182) at the S2-S3 linker relays the calmodulin signal from its inner boundary to the external pore to allow proper channel conduction. Thus, we revealed a unique mechanism of inactivation gating in Kv7.1, exquisitely controlled by external Ca(2+) and allosterically coupled by internal PIP2 and Ca(2+)-calmodulin.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。