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膜限定细胞信号复合物:G蛋白对离子通道的直接调控

Membrane-delimited cell signaling complexes: direct ion channel regulation by G proteins.

作者信息

Brown A M

机构信息

Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Membr Biol. 1993 Jan;131(2):93-104. doi: 10.1007/BF02791318.

DOI:10.1007/BF02791318
PMID:7680074
Abstract

Ion channels are signaling molecules and by themselves perform no work. In this regard they are unlike the usual membrane enzyme effectors for G proteins. The pathways of G protein receptor, G protein and ion channels are, therefore, purely informational in function. Because a single G protein may have several ion channels as effectors, the effects should be coordinated and this seems to be the case. Inhibition of Ca2+ current and stimulation of K+ currents would have a greater impact than either alone. Additional flexibility is provided by spontaneous noise in the complexes of G protein receptor, G protein, and ion channel. By having a non-zero setpoint, the range of control is extended and the responses become bi-directional.

摘要

离子通道是信号分子,自身并不执行任何功。在这方面,它们不同于通常作为G蛋白膜酶效应器的分子。因此,G蛋白受体、G蛋白和离子通道的途径在功能上纯粹是信息性的。由于单个G蛋白可能有多个离子通道作为效应器,这些效应应该是协同的,似乎确实如此。抑制Ca2+电流和刺激K+电流比单独任何一种情况都有更大的影响。G蛋白受体、G蛋白和离子通道复合物中的自发噪声提供了额外的灵活性。通过设定一个非零的设定点,控制范围得以扩展,反应变得双向。

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Pertussis toxin substrate, the putative Ni component of adenylyl cyclases, is an alpha beta heterodimer regulated by guanine nucleotide and magnesium.百日咳毒素底物,即腺苷酸环化酶假定的镍成分,是一种受鸟嘌呤核苷酸和镁调节的αβ异二聚体。
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