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环核苷酸门控通道。激活的分子机制。

Cyclic nucleotide-gated channels. Molecular mechanisms of activation.

作者信息

Broillet M C, Firestein S

机构信息

Institut de Pharmacologie et de Toxicologie, Université de Lausanne, Switzerland.

出版信息

Ann N Y Acad Sci. 1999 Apr 30;868:730-40. doi: 10.1111/j.1749-6632.1999.tb11352.x.

Abstract

Activation of cyclic nucleotide-gated (CNG) channels represents the final step in the transduction pathways in both vision and olfaction. Over the past several years, CNG channels have been found in a variety of other cell types where they might fulfill various physiological functions. The olfactory and photoreceptor CNG channels rely on the binding of at least two molecules of cAMP or cGMP at intracellular sites on the channel protein to open a nonspecific cation conductance with a significant permeability to Ca ions. A series of elegant experiments with cloned channels and chimeric constructs has revealed significant information regarding the binding and gating reactions that lead to CNG channel activation. These recent studies have identified several regions as well as specific amino acid residues distributed on the retinal or the olfactory CNG channel subunits that play a key role in channel regulation. In this review, we will focus on these specific molecular sites of activation and modulation of CNG channels.

摘要

环核苷酸门控(CNG)通道的激活是视觉和嗅觉转导通路的最后一步。在过去几年中,人们在多种其他细胞类型中发现了CNG通道,它们可能在其中发挥各种生理功能。嗅觉和光感受器CNG通道依赖于通道蛋白胞内位点上至少两个环磷酸腺苷(cAMP)或环磷酸鸟苷(cGMP)分子的结合,以打开对钙离子具有显著通透性的非特异性阳离子电导。一系列使用克隆通道和嵌合构建体的精妙实验揭示了有关导致CNG通道激活的结合和门控反应的重要信息。这些最新研究已经确定了视网膜或嗅觉CNG通道亚基上分布的几个区域以及特定氨基酸残基,它们在通道调节中起关键作用。在本综述中,我们将聚焦于CNG通道激活和调节的这些特定分子位点。

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