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K 通道的高分辨率结构。

High-Resolution Structures of K Channels.

机构信息

Laboratory of Molecular Physiology and Biophysics and the Cryo-EM Center, Hauptmann-Woodward Medical Research Institute, Buffalo, NY, USA.

Department of Medicinal Chemistry, University of Florida, Gainesville, FL, USA.

出版信息

Handb Exp Pharmacol. 2021;267:51-81. doi: 10.1007/164_2021_454.

Abstract

Potassium channels are present in every living cell and essential to setting up a stable, non-zero transmembrane electrostatic potential which manifests the off-equilibrium livelihood of the cell. They are involved in other cellular activities and regulation, such as the controlled release of hormones, the activation of T-cells for immune response, the firing of action potential in muscle cells and neurons, etc. Pharmacological reagents targeting potassium channels are important for treating various human diseases linked to dysfunction of the channels. High-resolution structures of these channels are very useful tools for delineating the detailed chemical basis underlying channel functions and for structure-based design and optimization of their pharmacological and pharmaceutical agents. Structural studies of potassium channels have revolutionized biophysical understandings of key concepts in the field - ion selectivity, conduction, channel gating, and modulation, making them multi-modality targets of pharmacological regulation. In this chapter, I will select a few high-resolution structures to illustrate key structural insights, proposed allostery behind channel functions, disagreements still open to debate, and channel-lipid interactions and co-evolution. The known structural consensus allows the inference of conserved molecular mechanisms shared among subfamilies of K channels and makes it possible to develop channel-specific pharmaceutical agents.

摘要

钾通道存在于每个活细胞中,对于建立稳定的、非零的跨膜静电势至关重要,这种跨膜静电势表现出细胞的非平衡状态。钾通道还参与其他细胞活动和调节,如激素的受控释放、T 细胞的免疫反应激活、肌肉细胞和神经元动作电位的触发等。针对钾通道的药理学试剂对于治疗与通道功能障碍相关的各种人类疾病非常重要。这些通道的高分辨率结构是阐明通道功能基础的详细化学基础的非常有用的工具,也是基于结构设计和优化其药理学和药物制剂的重要工具。钾通道的结构研究彻底改变了生物物理领域的关键概念的理解——离子选择性、传导、通道门控和调节,使它们成为多模态药理学调节的靶点。在本章中,我将选择几个高分辨率结构来阐明关键的结构见解、通道功能背后的变构假设、仍存在争议的问题,以及通道-脂质相互作用和共同进化。已知的结构共识允许推断 K 通道亚家族之间共享的保守分子机制,并使开发通道特异性药物制剂成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ea4/9382700/b63d8923426e/nihms-1827460-f0001.jpg

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本文引用的文献

1
Ball-and-chain inactivation in a calcium-gated potassium channel.钙离子门控钾通道中的球链失活。
Nature. 2020 Apr;580(7802):288-293. doi: 10.1038/s41586-020-2116-0. Epub 2020 Mar 18.
2
Ion permeation in potassium ion channels.钾离子通道中的离子渗透。
Acta Crystallogr D Struct Biol. 2020 Apr 1;76(Pt 4):326-331. doi: 10.1107/S2059798320003599.
5
10
Structural Basis of Nav1.7 Inhibition by a Gating-Modifier Spider Toxin.Nav1.7 通道调制型蜘蛛毒素抑制的结构基础。
Cell. 2019 Feb 7;176(4):702-715.e14. doi: 10.1016/j.cell.2018.12.018. Epub 2019 Jan 17.

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