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来自织锦芋螺的一种选择性靶向神经元烟碱型乙酰胆碱受体亚型的T-超家族芋螺毒素TxVC的特性分析。

Characterization of a T-superfamily conotoxin TxVC from Conus textile that selectively targets neuronal nAChR subtypes.

作者信息

Wang Shuo, Du Tianpeng, Liu Zhuguo, Wang Sheng, Wu Ying, Ding Jiuping, Jiang Ling, Dai Qiuyun

机构信息

Beijing Institute of Biotechnology, Beijing 10071, China.

Key Laboratory of Magnetic Resonance in Biological Systems, National Center for Magnetic Resonance in Wuhan, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Science, Wuhan 430071, China.

出版信息

Biochem Biophys Res Commun. 2014 Nov 7;454(1):151-6. doi: 10.1016/j.bbrc.2014.10.055. Epub 2014 Oct 18.

Abstract

T-superfamily conotoxins have a typical cysteine pattern of "CC-CC", and are known to mainly target calcium or sodium ion channels. Recently, we screened the targets of a series of T-superfamily conotoxins and found that a new T-superfamily conotoxin TxVC (KPCCSIHDNSCCGL-NH2) from the venom of Conus textile. It selectively targeted the neuronal nicotinic acetylcholine receptor (nAChR) subtypes α4β2 and α3β2, with IC50 values of 343.4 and 1047.2nM, respectively, but did not exhibit obvious pharmacological effects on voltage-gated potassium, sodium or calcium channel in DRG cells, the BK channels expressed in HEK293 cells, or the Kv channels in LβT2 cells. The changes in the inhibitory activities of its Ala mutants, the NMR structure, and molecular simulation results based on other conotoxins targeting nAChR α4β2, all demonstrated that the residues Ile(6) and Leu(14) were the main hydrophobic pharmacophores. To our best knowledge, this is the first T-superfamily conotoxin that inhibits neuronal nAChRs and possesses high binding affinity to α4β2. This finding will expand the knowledge of the targets of T-superfamily conotoxins and the motif information could help the design of new nAChR inhibitors.

摘要

T超家族芋螺毒素具有典型的“CC - CC”半胱氨酸模式,已知主要作用于钙或钠离子通道。最近,我们筛选了一系列T超家族芋螺毒素的作用靶点,发现了一种来自织锦芋螺毒液的新型T超家族芋螺毒素TxVC(KPCCSIHDNSCCGL - NH2)。它选择性地作用于神经元烟碱型乙酰胆碱受体(nAChR)亚型α4β2和α3β2,IC50值分别为343.4和1047.2nM,但对背根神经节(DRG)细胞中的电压门控钾、钠或钙通道、HEK293细胞中表达的大电导钙激活钾(BK)通道或LβT2细胞中的钾通道(Kv)均未表现出明显的药理作用。其丙氨酸突变体抑制活性的变化、核磁共振(NMR)结构以及基于其他作用于nAChR α4β2的芋螺毒素的分子模拟结果均表明,异亮氨酸(Ile(6))和亮氨酸(Leu(14))残基是主要的疏水药效基团。据我们所知,这是首个抑制神经元nAChRs且对α4β2具有高结合亲和力的T超家族芋螺毒素。这一发现将拓展对T超家族芋螺毒素作用靶点的认识,且该基序信息有助于新型nAChR抑制剂的设计。

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