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KCNE1与KCNQ1孔道结合以调节钾通道活性。

KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity.

作者信息

Melman Yonathan F, Um Sung Yon, Krumerman Andrew, Kagan Anna, McDonald Thomas V

机构信息

Department of Medicine, Department of Molecular Pharmacology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

出版信息

Neuron. 2004 Jun 24;42(6):927-37. doi: 10.1016/j.neuron.2004.06.001.

Abstract

Potassium channels control the resting membrane potential and excitability of biological tissues. Many voltage-gated potassium channels are controlled through interactions with accessory subunits of the KCNE family through mechanisms still not known. Gating of mammalian channel KCNQ1 is dramatically regulated by KCNE subunits. We have found that multiple segments of the channel pore structure bind to the accessory protein KCNE1. The sites that confer KCNE1 binding are necessary for the functional interaction, and all sites must be present in the channel together for proper regulation by the accessory subunit. Specific gating control is localized to a single site of interaction between the ion channel and accessory subunit. Thus, direct physical interaction with the ion channel pore is the basis of KCNE1 regulation of K+ channels.

摘要

钾通道控制生物组织的静息膜电位和兴奋性。许多电压门控钾通道是通过与KCNE家族辅助亚基的相互作用来控制的,其机制尚不清楚。哺乳动物通道KCNQ1的门控受KCNE亚基的显著调节。我们发现通道孔结构的多个片段与辅助蛋白KCNE1结合。赋予KCNE1结合的位点对于功能相互作用是必需的,并且所有位点必须同时存在于通道中才能由辅助亚基进行适当调节。特定的门控控制定位于离子通道和辅助亚基之间的单个相互作用位点。因此,与离子通道孔的直接物理相互作用是KCNE1对钾通道调节的基础。

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