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人类瞬时受体电位锚蛋白 1 通道:结构、功能和生理学。

Human Transient Receptor Potential Ankyrin 1 Channel: Structure, Function, and Physiology.

机构信息

Department of Cellular Neurophysiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.

Division of Biomolecular Physics, Institute of Physics, Faculty of Mathematics and Physics, Charles University, Prague, Czech Republic.

出版信息

Subcell Biochem. 2024;104:207-244. doi: 10.1007/978-3-031-58843-3_10.


DOI:10.1007/978-3-031-58843-3_10
PMID:38963489
Abstract

The transient receptor potential ion channel TRPA1 is a Ca-permeable nonselective cation channel widely expressed in sensory neurons, but also in many nonneuronal tissues typically possessing barrier functions, such as the skin, joint synoviocytes, cornea, and the respiratory and intestinal tracts. Here, the primary role of TRPA1 is to detect potential danger stimuli that may threaten the tissue homeostasis and the health of the organism. The ability to directly recognize signals of different modalities, including chemical irritants, extreme temperatures, or osmotic changes resides in the characteristic properties of the ion channel protein complex. Recent advances in cryo-electron microscopy have provided an important framework for understanding the molecular basis of TRPA1 function and have suggested novel directions in the search for its pharmacological regulation. This chapter summarizes the current knowledge of human TRPA1 from a structural and functional perspective and discusses the complex allosteric mechanisms of activation and modulation that play important roles under physiological or pathophysiological conditions. In this context, major challenges for future research on TRPA1 are outlined.

摘要

瞬时受体电位离子通道 TRPA1 是一种 Ca2+通透性非选择性阳离子通道,广泛表达于感觉神经元,但也表达于许多具有屏障功能的非神经元组织中,如皮肤、关节滑膜细胞、角膜以及呼吸道和肠道。在这里,TRPA1 的主要作用是检测可能威胁组织内稳态和机体健康的潜在危险刺激。其能够直接识别不同模态的信号,包括化学刺激物、极端温度或渗透压变化,这归因于离子通道蛋白复合物的特征属性。低温电子显微镜技术的最新进展为理解 TRPA1 功能的分子基础提供了重要框架,并为其药理学调控的探索提供了新的方向。本章从结构和功能的角度总结了人类 TRPA1 的现有知识,并讨论了在生理或病理生理条件下发挥重要作用的复杂变构激活和调节机制。在此背景下,概述了未来 TRPA1 研究的主要挑战。

相似文献

[1]
Human Transient Receptor Potential Ankyrin 1 Channel: Structure, Function, and Physiology.

Subcell Biochem. 2024

[2]
The transient receptor potential channel TRPA1: from gene to pathophysiology.

Pflugers Arch. 2012-9-22

[3]
Mammalian Transient Receptor Potential TRPA1 Channels: From Structure to Disease.

Physiol Rev. 2019-10-31

[4]
Activation characteristics of transient receptor potential ankyrin 1 and its role in nociception.

Am J Physiol Cell Physiol. 2011-6-8

[5]
Transient Receptor Potential Channel Ankyrin 1: A Unique Regulator of Vascular Function.

Cells. 2021-5-11

[6]
TRPA1: a molecular view.

J Neurophysiol. 2018-11-28

[7]
Structure of the TRPA1 ion channel suggests regulatory mechanisms.

Nature. 2015-4-23

[8]
Sample preparation of the human TRPA1 ion channel for cryo-EM studies.

Methods Enzymol. 2021

[9]
Structural insights into the molecular mechanism of mouse TRPA1 activation and inhibition.

J Gen Physiol. 2018-4-27

[10]
TRPA1 channels: molecular sentinels of cellular stress and tissue damage.

J Physiol. 2016-8-1

本文引用的文献

[1]
Transient receptor potential ankyrin 1 (TRPA1) modulators: Recent update and future perspective.

Eur J Med Chem. 2023-9-5

[2]
Molecular mechanism of hyperactivation conferred by a truncation of TRPA1.

Nat Commun. 2023-5-19

[3]
Molecular architecture and gating mechanisms of the Drosophila TRPA1 channel.

Cell Discov. 2023-4-4

[4]
Using evolutionary data to make sense of macromolecules with a "face-lifted" ConSurf.

Protein Sci. 2023-3

[5]
Visualization of translation and protein biogenesis at the ER membrane.

Nature. 2023-2

[6]
Bipartite Activation of Sensory Neurons by a TRPA1 Agonist Allyl Isothiocyanate Is Reflected by Complex Ca Influx and CGRP Release Patterns: Enhancement by NGF and Inhibition with VAMP and SNAP-25 Cleaving Botulinum Neurotoxins.

Int J Mol Sci. 2023-1-10

[7]
Discovery of , a Selective CNS Penetrant Chemical Probe as Transient Receptor Potential Ankyrin 1 (TRPA1) Antagonist.

J Med Chem. 2023-1-26

[8]
Structural and functional analyses of a GPCR-inhibited ion channel TRPM3.

Neuron. 2023-1-4

[9]
The human TRPA1 intrinsic cold and heat sensitivity involves separate channel structures beyond the N-ARD domain.

Nat Commun. 2022-10-17

[10]
Atomistic mechanisms of human TRPA1 activation by electrophile irritants through molecular dynamics simulation and mutual information analysis.

Sci Rep. 2022-3-23

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