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内向整流钾通道的细胞内调节

Intracellular regulation of inward rectifier K+ channels.

作者信息

Ruppersberg J P

机构信息

Dept. of Physiology II, University of Tübingen, Germany.

出版信息

Pflugers Arch. 2000 Nov;441(1):1-11. doi: 10.1007/s004240000380.

Abstract

Inward rectifier potassium (Kir) channels comprise a relatively young gene family of ion channels whose first member was isolated in 1993. A common property its members share is a strong dependence on intracellular regulators such as polyamines, nucleotides, phospholipids, kinases, pH and guanosine-triphosphate-binding proteins (G-proteins). The physiological role of Kir channels is to modulate the excitability and secretion of potassium (K+) to maintain K+ homeostasis, under the control of various intracellular second messengers. Structurally, Kir channels are assembled from four alpha-subunits each carrying the prototypic K+-channel pore region lined by two transmembrane segments with intracellular N- and C-termini. The exact molecular mechanism of Kir channel gating by intracellular second messengers is of considerable biophysical interest. Recent studies have gained significant insight into the molecular mechanism of intracellular regulation by pH. This review illustrates the various modes of regulation of this class of ion channel and the present knowledge of the underlying molecular mechanisms.

摘要

内向整流钾(Kir)通道构成了一个相对年轻的离子通道基因家族,其首个成员于1993年被分离出来。该家族成员的一个共同特性是对细胞内调节因子有很强的依赖性,这些调节因子包括多胺、核苷酸、磷脂、激酶、pH值和鸟苷三磷酸结合蛋白(G蛋白)。Kir通道的生理作用是在各种细胞内第二信使的控制下,调节钾(K+)的兴奋性和分泌,以维持K+稳态。在结构上,Kir通道由四个α亚基组装而成,每个亚基都带有由两个跨膜片段构成的原型K+通道孔区域,其N端和C端位于细胞内。细胞内第二信使对Kir通道门控的确切分子机制具有相当大的生物物理学研究价值。最近的研究对pH值介导的细胞内调节分子机制有了重要的认识。本综述阐述了这类离子通道的各种调节模式以及对潜在分子机制的当前认识。

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