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蜈蚣毒素导致伤害感受器 TRPV1 离子通道快速脱敏。

A centipede toxin causes rapid desensitization of nociceptor TRPV1 ion channel.

机构信息

Department of Pharmacology, Qingdao University School of Pharmacy, Qingdao, Shandong, China; Department of Biophysics and Kidney Disease Center, The First Affiliated Hospital, Institute of Neuroscience, National Health Commission and Chinese Academy of Medical Sciences Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang Province, China.

Department of Biophysics and Kidney Disease Center, The First Affiliated Hospital, Institute of Neuroscience, National Health Commission and Chinese Academy of Medical Sciences Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang Province, China.

出版信息

Toxicon. 2020 Apr 30;178:41-49. doi: 10.1016/j.toxicon.2020.02.016. Epub 2020 Feb 22.

Abstract

The nociceptive transient receptor potential vanilloid 1 (TRPV1) ion channel is a polymodal receptor for multiple painful stimuli, hence actively pursued as a target for analgesic drugs. We identified a small peptide toxin RhTx2 from the Chinese red-headed centipede that strongly modulates TRPV1 activities. RhTx2, a 31-amino-acid peptide, is similar to a TRPV1-activating toxin RhTx we have previously discovered but with four extra amino acids at the N terminus. We observed that, like RhTx, RhTx2 activated TRPV1, but RhTx2 rapidly desensitized the channel upon prolonged exposure. Desensitization was achieved by reducing both the open probability and the single-channel conductance. RhTx2 is not only a tool to study the desensitization mechanism of TRPV1, but also a promising starting molecule for developing novel analgesics.

摘要

伤害性瞬时受体电位香草酸 1(TRPV1)离子通道是多种疼痛刺激的多模态受体,因此被积极用作镇痛药物的靶点。我们从中国红头蜈蚣中鉴定出一种名为 RhTx2 的小肽毒素,它强烈调节 TRPV1 的活性。RhTx2 是一种 31 个氨基酸的肽,与我们之前发现的 TRPV1 激活毒素 RhTx 相似,但 N 端有四个额外的氨基酸。我们观察到,与 RhTx 一样,RhTx2 激活 TRPV1,但 RhTx2 在长时间暴露后会迅速脱敏该通道。脱敏通过降低通道的开放概率和单通道电导来实现。RhTx2 不仅是研究 TRPV1 脱敏机制的工具,也是开发新型镇痛药的有前途的起始分子。

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