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蛇毒中“功能位点”残基的变异及三指神经毒素的分类

Variations in "Functional Site" Residues and Classification of Three-Finger Neurotoxins in Snake Venoms.

作者信息

Kini R Manjunatha, Koh Cho Yeow

机构信息

Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore 117558, Singapore.

Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore.

出版信息

Toxins (Basel). 2025 Jul 24;17(8):364. doi: 10.3390/toxins17080364.

Abstract

Three-finger toxins (3FTxs) are the largest group of nonenzymatic toxins found in snake venoms. Among them, neurotoxins that target nicotinic acetylcholine receptors are the most well-studied ligands. In addition to the classical neurotoxins, several other new classes have been characterized for their structure, receptor subtype, and species selectivity. Here, we systematically analyzed over 700 amino acid sequences of three-finger neurotoxins that interact with nicotinic acetylcholine receptors. Based on the amino acid residue substitutions in the functional sites and structural features of various classes of neurotoxins, we have classified them into over 150 distinct subgroups. Currently, only a small number of typical examples representing these subgroups have been studied for their structure, function, and subtype selectivity. The functional site residues responsible for their interaction with specific receptor subtypes of several toxins are yet to be identified. The molecular details of each subgroup representative toxin with its target receptor will contribute towards the understanding of subtype- and/or interface-selectivity. Thus, this review will provide new impetus in the toxin research and pave the way for the design of potent, selective ligands for nicotinic acetylcholine receptors.

摘要

三指毒素(3FTxs)是蛇毒中最大的非酶毒素组。其中,靶向烟碱型乙酰胆碱受体的神经毒素是研究最为深入的配体。除了经典的神经毒素外,其他几类新的神经毒素也已根据其结构、受体亚型和物种选择性进行了表征。在这里,我们系统地分析了700多个与烟碱型乙酰胆碱受体相互作用的三指神经毒素的氨基酸序列。基于各类神经毒素功能位点的氨基酸残基取代和结构特征,我们将它们分为150多个不同的亚组。目前,仅对代表这些亚组的少数典型例子进行了结构、功能和亚型选择性研究。几种毒素与特定受体亚型相互作用的功能位点残基尚未确定。每个亚组代表性毒素与其靶受体的分子细节将有助于理解亚型和/或界面选择性。因此,本综述将为毒素研究提供新的动力,并为设计强效、选择性的烟碱型乙酰胆碱受体配体铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18f/12390062/6059bf69ede5/toxins-17-00364-g001a.jpg

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