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一种从皮氏矛头蝮蛇毒中快速分离两种肌毒素——二聚体吡拉毒素-I和II的方法。N端测序。

A quick procedure for the isolation of dimeric piratoxins-I and II, two myotoxins from Bothrops pirajai snake venom. N-terminal sequencing.

作者信息

Toyama M H, Mancuso L C, Giglio J R, Novello J C, Oliveira B, Marangoni S

机构信息

Departamento de Bioquímica, Unicamp, Instituto de Biologia, Brasil.

出版信息

Biochem Mol Biol Int. 1995 Dec;37(6):1047-55.

PMID:8747534
Abstract

Two myotoxins, MP-I and MP-II, from Bothrops pirajai snake venom, have been purified by a quick high performance liquid chromatography (HPLC) procedure. Based on the HPLC coelution profile, amino acid composition, N-terminal sequence, polyacrylamide gel electrophoresis (PAGE) migration, as well as lack of phospholipase-A2 (PLA2) and proteolytic activities, MP-I and MP-II were identified as piratoxin-I (PrTX-I) and II (PrTX-II), respectively. This procedure affords, aside the reduced operation time, a high yield (35% of the applied sample in terms of A280nm) of MP-I, which is the major myotoxin of the venom. The N-terminal sequences of MP-I, MP-II, PrTX-I and PrTX-II, up to the 51st, 41st, 46th and 39th residues, respectively, have been determined, revealing MP-I (and hence PrTX-I) as a Lys-49 PLA2-like myotoxin. Both MP-I and MP-II have been shown, by SDS-PAGE, to occur in dimeric isoforms.

摘要

通过快速高效液相色谱(HPLC)法从皮氏矛头蝮蛇毒中纯化出了两种肌毒素MP-I和MP-II。基于HPLC共洗脱图谱、氨基酸组成、N端序列、聚丙烯酰胺凝胶电泳(PAGE)迁移情况,以及缺乏磷脂酶A2(PLA2)和蛋白水解活性,MP-I和MP-II分别被鉴定为皮拉毒素-I(PrTX-I)和皮拉毒素-II(PrTX-II)。该方法除了缩短操作时间外,还能以高产量(以A280nm计,占应用样品的35%)获得MP-I,它是蛇毒的主要肌毒素。已分别测定了MP-I、MP-II、PrTX-I和PrTX-II的N端序列,分别至第51、41、46和39个残基,结果表明MP-I(因此PrTX-I)是一种49位赖氨酸类似PLA2的肌毒素。通过SDS-PAGE已表明MP-I和MP-II均以二聚体异构体形式存在。

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