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环核苷酸门控通道

Cyclic nucleotide-gated channels.

作者信息

Biel Martin, Michalakis Stylianos

机构信息

Center for Integrated Protein Science CIPS-M and Zentrum für Pharmaforschung-Department Pharmazie, Pharmakologie für Naturwissenschaften, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, München, 81377, Germany.

出版信息

Handb Exp Pharmacol. 2009(191):111-36. doi: 10.1007/978-3-540-68964-5_7.

Abstract

Cyclic nucleotide-gated (CNG) channels are ion channels which are activated by the binding of cGMP or cAMP. The channels are important cellular switches which transduce changes in intracellular concentrations of cyclic nucleotides into changes of the membrane potential and the Ca2+ concentration. CNG channels play a central role in the signal transduction pathways of vision and olfaction. Structurally, the channels belong to the superfamily of pore-loop cation channels. They share a common domain structure with hyperpolarization-activated cyclic nucleotide-gated (HCN) channels and Eag-like K+ channels. In this chapter, we give an overview on the molecular properties of CNG channels and describe the signal transduction pathways these channels are involved in. We will also summarize recent insights into the physiological and pathophysiological role of CNG channel proteins that have emerged from the analysis of CNG channel-deficient mouse models and human channelopathies.

摘要

环核苷酸门控(CNG)通道是一类离子通道,可被环鸟苷酸(cGMP)或环腺苷酸(cAMP)结合激活。这些通道是重要的细胞开关,能将细胞内环核苷酸浓度的变化转化为膜电位和钙离子浓度的变化。CNG通道在视觉和嗅觉信号转导途径中起核心作用。在结构上,这些通道属于孔环阳离子通道超家族。它们与超极化激活的环核苷酸门控(HCN)通道和类Eag钾通道具有共同的结构域结构。在本章中,我们将概述CNG通道的分子特性,并描述这些通道所参与的信号转导途径。我们还将总结对CNG通道缺陷小鼠模型和人类通道病分析中得出的关于CNG通道蛋白生理和病理生理作用的最新见解。

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