Suppr超能文献

靶向疼痛信号转导中电压门控钠离子通道的蜘蛛和蝎子毒素 knottins。

Spider and scorpion knottins targeting voltage-gated sodium ion channels in pain signaling.

机构信息

College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, Hunan 410128, China.

School of Public Health & Laboratory Medicine, Hunan University of Medicine, Huaihua 418000, China.

出版信息

Biochem Pharmacol. 2024 Sep;227:116465. doi: 10.1016/j.bcp.2024.116465. Epub 2024 Aug 3.

Abstract

In sensory neurons that transmit pain signals, whether acute or chronic, voltage-gated sodium channels (VGSCs) are crucial for regulating excitability. Na1.1, Na1.3, Na1.6, Na1.7, Na1.8, and Na1.9 have been demonstrated and defined their functional roles in pain signaling based on their biophysical properties and distinct patterns of expression in each subtype of sensory neurons. Scorpions and spiders are traditional Chinese medicinal materials, belonging to the arachnid class. Most of the studied species of them have evolved venom peptides that exhibit a wide variety of knottins specifically targeting VGSCs with subtype selectivity and conformational specificity. This review provides an overview on the exquisite knottins from scorpion and spider venoms targeting pain-related Na channels, describing the sequences and the structural features as well as molecular determinants that influence their selectivity on special subtype and at particular conformation, with an aim for the development of novel research tools on Na channels and analgesics with minimal adverse effects.

摘要

在传递疼痛信号的感觉神经元中,无论是急性还是慢性疼痛,电压门控钠离子通道(VGSCs)对于调节兴奋性至关重要。Na1.1、Na1.3、Na1.6、Na1.7、Na1.8 和 Na1.9 已被证明,并根据其在每种感觉神经元亚型中的生物物理特性和表达模式定义了它们在疼痛信号转导中的功能作用。蝎子和蜘蛛是中药材,属于蛛形纲。它们的大多数研究物种已经进化出毒液肽,这些毒液肽表现出广泛的具有亚型选择性和构象特异性的 knottins,专门针对 VGSCs。本综述概述了来自蝎子和蜘蛛毒液的针对与疼痛相关的 Na 通道的精致 knottins,描述了序列和结构特征以及影响它们对特殊亚型和特定构象选择性的分子决定因素,旨在开发新型研究工具,用于研究 Na 通道和具有最小不良反应的镇痛药。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验