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原子分辨率下电压门控钠离子通道的结构与功能。

Structure and function of voltage-gated sodium channels at atomic resolution.

机构信息

W. A. Catterall: Department of Pharmacology, Box 357280, University of Washington, Seattle, WA 98195-7280, USA.

出版信息

Exp Physiol. 2014 Jan;99(1):35-51. doi: 10.1113/expphysiol.2013.071969. Epub 2013 Oct 4.

Abstract

Voltage-gated sodium channels initiate action potentials in nerve, muscle and other excitable cells. Early physiological studies described sodium selectivity, voltage-dependent activation and fast inactivation, and developed conceptual models for sodium channel function. This review article follows the topics of my 2013 Sharpey-Schafer Prize Lecture and gives an overview of research using a combination of biochemical, molecular biological, physiological and structural biological approaches that have elucidated the structure and function of sodium channels at the atomic level. Structural models for voltage-dependent activation, sodium selectivity and conductance, drug block and both fast and slow inactivation are discussed. A perspective for the future envisions new advances in understanding the structural basis for sodium channel function and the opportunity for structure-based discovery of novel therapeutics.

摘要

电压门控钠离子通道在神经、肌肉和其他可兴奋细胞中引发动作电位。早期的生理研究描述了钠离子的选择性、电压依赖性激活和快速失活,并为钠离子通道功能开发了概念模型。这篇综述文章遵循了我 2013 年 Sharpey-Schafer 奖演讲的主题,概述了使用生化、分子生物学、生理学和结构生物学方法的研究,这些方法阐明了钠离子通道在原子水平上的结构和功能。讨论了电压依赖性激活、钠离子选择性和电导、药物阻断以及快速和缓慢失活的结构模型。对未来的展望设想了在理解钠离子通道功能的结构基础方面取得新进展的机会,以及基于结构发现新型治疗药物的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d63/3885250/2fb20fe0b673/nihms532764f1.jpg

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