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在蝎毒中发现的一类新型肽,对大鼠外周和中枢神经系统具有神经抑制作用。

A novel class of peptide found in scorpion venom with neurodepressant effects in peripheral and central nervous system of the rat.

作者信息

Corona Miguel, Coronas Fredy V, Merino Enrique, Becerril Baltazar, Gutiérrez Rafael, Rebolledo-Antunez Santiago, Garcia David E, Possani Lourival D

机构信息

Institute of Biotechnology, National Autonomous University of Mexico, Avenida Universidad, 2001, Apartado Postal 510-3 Cuernavaca 62210, Mexico.

出版信息

Biochim Biophys Acta. 2003 Jun 26;1649(1):58-67. doi: 10.1016/s1570-9639(03)00155-9.

Abstract

A novel toxin, named Cll9, was isolated from the venom of the scorpion Centruroides limpidus limpidus Karsch. It is composed of 63 amino acid residues closely packed by four disulfide bridges. It showed no apparent effect when injected to insects, crustaceans and i.p. to mice. However, when i.c.v. injected in the rat it immediately induced sleep, suggesting that it has a neurodepressant effect. We confirmed this by showing that it has a strong antiepileptic action, as assessed with the penicillin focus model. Its effectiveness in inhibiting Na(+) permeability in (cultured) rat peripheral ganglia further supports its neurodepressant actions. However, this peptide did not affect other Na(+) channels such as those from cerebellum granular cells in culture or the rSkM1 Na(+) channels expressed in HEK293. The cDNA and genomic regions encoding this peptide were cloned and sequenced. This peptide is synthesized as a precursor of 84 amino acid residues and processed by removing 19 amino acids (signal peptide) from the amino terminal region and a couple of lysine residues from the carboxyl end. The presence of an intron of 777 bases interrupting the region encoding the signal peptide was also revealed. A comparison of its primary sequence, with more than 100 scorpion toxins known, showed that together with toxin CsE9 they constitute a new subfamily of peptides considered to be one of the most divergent groups of scorpion toxin-like peptides discovered.

摘要

从墨西哥金背蝎(Centruroides limpidus limpidus Karsch)毒液中分离出一种名为Cll9的新型毒素。它由63个氨基酸残基组成,通过四个二硫键紧密排列。将其注射到昆虫、甲壳类动物体内以及对小鼠进行腹腔注射时,未显示出明显效果。然而,当对大鼠进行脑室内注射时,它会立即诱导睡眠,这表明它具有神经抑制作用。我们通过青霉素病灶模型评估证实它具有强大的抗癫痫作用,从而进一步确认了这一点。它在抑制(培养的)大鼠外周神经节中钠(+)通透性方面的有效性进一步支持了其神经抑制作用。然而,这种肽并不影响其他钠(+)通道,如培养的小脑颗粒细胞中的通道或在HEK293中表达的rSkM1钠(+)通道。编码该肽的cDNA和基因组区域已被克隆和测序。该肽作为一个84个氨基酸残基的前体进行合成,并通过从氨基末端区域去除19个氨基酸(信号肽)以及从羧基末端去除几个赖氨酸残基进行加工。还发现存在一个777个碱基的内含子,它中断了编码信号肽的区域。将其一级序列与100多种已知的蝎子毒素进行比较,结果表明它与毒素CsE9一起构成了一个新的肽亚家族,被认为是发现的蝎子毒素样肽中最具差异的群体之一。

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