多足类动物大范围热感受器的结构和功能

Xiaoying Chen, Licheng Yuan, Han Wen, Qingxia Ma, Zhenfeng Deng, Yongan Xu, Zhihao Yao, Yunfei Wang, Shilong Yang, Nannan Su, Fan Yang
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引用次数: 0

摘要

宽范围热受体1 (BRTNaC1)在低细胞外pH下被热激活,最近在多足类动物中被发现。尽管BRTNaC1的过表达会导致具有阳离子选择性的强热激活电流,但该受体的结构以及它如何被质子和热门控仍有待研究。在这里,我们测定了BRTNaC1在载脂蛋白、质子诱导和加热状态下的低温电镜结构。基于这些结构,膜片钳记录和分子动力学模拟,我们发现BRTNaC1的质子激活使用了“扭手腕”机制,而热量诱导BRTNaC1的广泛构象变化,包括跨膜螺旋的旋转和移动以打开该通道。此外,由于睾酮抑制BRTNaC1的激活,我们确定了四个簇状残基对这种抑制很重要。因此,我们的研究奠定了BRTNaC1离子通道中配体和温度门控的结构基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Structure and function of a broad-range thermal receptor in myriapods

Structure and function of a broad-range thermal receptor in myriapods

Broad-range thermal receptor 1 (BRTNaC1), activated by heat at low extracellular pH, was recently identified in myriapods. Although the overexpression of BRTNaC1 leads to robust heat-activated current with a cation selectivity profile, the structure of this receptor and how it is gated by proton and heat remain to be investigated. Here we determine cryogenic electron microscopy structures of BRTNaC1 in the apo, proton-induced and heated states. Based on these structures, patch-clamp recordings and molecular dynamic simulations, we found that a ‘twist the wrist’ mechanism is used for proton activation of BRTNaC1, while heat induces broad conformational changes in BRTNaC1, including rotation and shift in the transmembrane helices to open this channel. Moreover, as testosterone inhibited BRTNaC1 activation, we identified four clustered residues important for such inhibition. Therefore, our study has established the structural basis for ligand and temperature gating in the BRTNaC1 ion channel.

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