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Shaker钾离子通道的组成性激活。

Constitutive activation of the Shaker Kv channel.

作者信息

Sukhareva Manana, Hackos David H, Swartz Kenton J

机构信息

Molecular Physiology and Biophysics Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892. email:

出版信息

J Gen Physiol. 2003 Nov;122(5):541-56. doi: 10.1085/jgp.200308905. Epub 2003 Oct 13.

Abstract

In different types of K+ channels the primary activation gate is thought to reside near the intracellular entrance to the ion conduction pore. In the Shaker Kv channel the gate is closed at negative membrane voltages, but can be opened with membrane depolarization. In a previous study of the S6 activation gate in Shaker (Hackos, D.H., T.H. Chang, and K.J. Swartz. 2002. J. Gen. Physiol. 119:521-532.), we found that mutation of Pro 475 to Asp results in a channel that displays a large macroscopic conductance at negative membrane voltages, with only small increases in conductance with membrane depolarization. In the present study we explore the mechanism underlying this constitutively conducting phenotype using both macroscopic and single-channel recordings, and probes that interact with the voltage sensors or the intracellular entrance to the ion conduction pore. Our results suggest that constitutive conduction results from a dramatic perturbation of the closed-open equilibrium, enabling opening of the activation gate without voltage-sensor activation. This mechanism is discussed in the context of allosteric models for activation of Kv channels and what is known about the structure of this critical region in K+ channels.

摘要

在不同类型的钾离子通道中,主要的激活门被认为位于离子传导孔的细胞内入口附近。在摇椅式钾离子通道(Shaker Kv channel)中,该门在膜电位为负时关闭,但可随膜去极化而打开。在之前一项关于摇椅式通道中S6激活门的研究中(哈科斯,D.H.,T.H. 张,以及K.J. 斯沃茨。2002年。《普通生理学杂志》119:521 - 532),我们发现将475位的脯氨酸突变为天冬氨酸会导致通道在膜电位为负时呈现出较大的宏观电导,而随着膜去极化,电导仅有小幅增加。在本研究中,我们使用宏观和单通道记录以及与电压传感器或离子传导孔的细胞内入口相互作用的探针,探究这种组成型传导表型背后的机制。我们的结果表明,组成型传导是由于关闭 - 开放平衡的剧烈扰动所致,使得激活门在电压传感器未激活的情况下就能打开。我们将在钾离子通道激活的变构模型以及关于钾离子通道这一关键区域结构的已知信息的背景下讨论这一机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3459/2229584/291ef62b7f89/200308905f1.jpg

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