Suppr超能文献

Kv1.6 对 Kv1.4 通道 N 型失活的位置依赖性衰减。

Position-dependent attenuation by Kv1.6 of N-type inactivation of Kv1.4-containing channels.

机构信息

International Centre for Neurotherapeutics, Dublin City University, Glasnevin, Ireland.

出版信息

Biochem J. 2011 Sep 1;438(2):389-96. doi: 10.1042/BJ20102169.

Abstract

Assembly of distinct α subunits of Kv1 (voltage-gated K(+) channels) into tetramers underlies the diversity of their outward currents in neurons. Kv1.4-containing channels normally exhibit N-type rapid inactivation, mediated through an NIB (N-terminal inactivation ball); this can be over-ridden if associated with a Kv1.6 α subunit, via its NIP (N-type inactivation prevention) domain. Herein, NIP function was shown to require positioning of Kv1.6 adjacent to the Kv1.4 subunit. Using a recently devised gene concatenation, heterotetrameric Kv1 channels were expressed as single-chain proteins on the plasmalemma of HEK (human embryonic kidney)-293 cells, so their constituents could be arranged in different positions. Placing the Kv1.4 and 1.6 genes together, followed by two copies of Kv1.2, yielded a K(+) current devoid of fast inactivation. Mutation of critical glutamates within the NIP endowed rapid inactivation. Moreover, separating Kv1.4 and 1.6 with a copy of Kv1.2 gave a fast-inactivating K(+) current with steady-state inactivation shifted to more negative potentials and exhibiting slower recovery, correlating with similar inactivation kinetics seen for Kv1.4-(1.2)(3). Alternatively, separating Kv1.4 and 1.6 with two copies of Kv1.2 yielded slow-inactivating currents, because in this concatamer Kv1.4 and 1.6 should be together. These findings also confirm that the gene concatenation can generate K(+) channels with α subunits in pre-determined positions.

摘要

不同的 Kv1(电压门控 K(+)通道)α 亚基组装成四聚体是神经元外向电流多样性的基础。Kv1.4 通道通常表现为 N 型快速失活,通过 NIB(N 端失活球)介导;如果与 Kv1.6α 亚基相关联,则通过其 NIP(N 型失活预防)结构域可以覆盖这种失活。在此,NIP 功能被证明需要将 Kv1.6 定位在 Kv1.4 亚基附近。使用最近设计的基因串联,异源四聚体 Kv1 通道作为单个链蛋白在 HEK(人胚肾)-293 细胞的质膜上表达,因此可以将它们的成分排列在不同的位置。将 Kv1.4 和 1.6 基因放在一起,然后是两个 Kv1.2 拷贝,得到的 K(+)电流没有快速失活。在 NIP 内的关键谷氨酸突变赋予快速失活。此外,用 Kv1.2 的一个拷贝将 Kv1.4 和 1.6 分开,会产生快速失活的 K(+)电流,稳态失活向更负的电位转移,并表现出较慢的恢复,与 Kv1.4-(1.2)(3) 中观察到的类似失活动力学相关。或者,用两个 Kv1.2 拷贝将 Kv1.4 和 1.6 分开,会产生缓慢失活的电流,因为在这个串联体中,Kv1.4 和 1.6 应该在一起。这些发现还证实,基因串联可以生成具有预先确定位置的α亚基的 K(+)通道。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验