Department of Physiology, Campus Gasthuisberg, Katholieke Universiteit Leuven, Leuven, Belgium.
J Physiol. 2011 Apr 1;589(Pt 7):1543-9. doi: 10.1113/jphysiol.2010.200717. Epub 2010 Nov 15.
Transient receptor potential (TRP) channels have been extensively studied over the past years. Yet, in most cases, the gating mechanisms of these polymodal cation channels still remain a puzzle. Using the nociceptive channel TRPA1 as an example, we discuss the role of dynamic regulation of the pore size (pore dilatation) on channel gating. Additionally, we critically revise current knowledge of the role of intracellular domains, such as ankyrin repeats and EF hand motifs, in channel activation and function. Finally, we assess some problems inherent to activation of TRPA1 by the reaction of electrophilic compounds with the nucleophilic thiol sink of N-terminal reactive cysteines.
在过去的几年中,瞬时受体电位 (TRP) 通道得到了广泛的研究。然而,在大多数情况下,这些多模态阳离子通道的门控机制仍然是一个谜。本文以痛觉通道 TRPA1 为例,讨论了孔径动态调节(孔扩张)对通道门控的作用。此外,还批判性地回顾了细胞内结构域(如锚蛋白重复序列和 EF 手模体)在通道激活和功能中的作用的现有知识。最后,评估了亲电化合物与 N 端反应性半胱氨酸的亲核巯基陷阱反应激活 TRPA1 所固有的一些问题。