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离子通道在膜微区的靶向定位:钾离子通道在脂筏中的定位

Targeting of ion channels to membrane microdomains: localization of KV channels to lipid rafts.

作者信息

Martens Jeffrey R, O'Connell Kristen, Tamkun Michael

机构信息

Department of Physiology and Pharmacology, Oregon Health Sciences University,Portland, OR 97201, USA.

出版信息

Trends Pharmacol Sci. 2004 Jan;25(1):16-21. doi: 10.1016/j.tips.2003.11.007.

Abstract

Voltage-gated K(+) channels are an important determinant of cellular excitability and key components of multiple signal transduction pathways. However, relatively little is known about the mechanisms of K(V) channel localization or their membrane partitioning. Lipid rafts are specialized membrane microdomains that are rich in sphingolipids and cholesterol. These rafts have been implicated in the organization of many membrane-associated signaling pathways and are currently the focus of intense interest in the scientific community. Biochemical and functional evidence indicate that K(V) channels, in addition to other ion channels, localize to lipid raft microdomains on the cell surface. Although several important questions regarding specific mechanisms of channel localization remain, emerging data indicate that protein-lipid interactions should be considered as a new mechanism of ion channel localization and compartmentation that might permit the therapeutic modulation of channel properties via alteration in membrane lipids.

摘要

电压门控钾离子通道是细胞兴奋性的重要决定因素,也是多种信号转导途径的关键组成部分。然而,对于钾离子通道定位机制及其膜分配情况,人们了解得相对较少。脂筏是富含鞘脂和胆固醇的特殊膜微区。这些脂筏与许多膜相关信号转导途径的组织有关,目前是科学界的研究热点。生化和功能证据表明,钾离子通道以及其他离子通道定位于细胞表面的脂筏微区。尽管关于通道定位的具体机制仍有几个重要问题有待解决,但新出现的数据表明,蛋白质 - 脂质相互作用应被视为离子通道定位和区室化的一种新机制,这可能允许通过改变膜脂质来对通道特性进行治疗性调节。

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