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对由来自南美巨蝮毒液的两种巴曲毒素B同工型形成的四聚体磷脂酶A2进行的初步X射线晶体学研究。

Preliminary X-ray crystallographic studies of a tetrameric phospholipase A2 formed by two isoforms of crotoxin B from Crotalus durissus terrificus venom.

作者信息

Marchi-Salvador D P, Corrêa L C, Salvador G H M, Magro A J, Oliveira C Z, Iulek J, Soares A M, Fontes M R M

机构信息

Departamento de Física e Biofísica, Instituto de Biociências, UNESP, CP 510, 18618-000 Botucatu-SP, Brazil.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Dec 1;63(Pt 12):1067-9. doi: 10.1107/S1744309107058563. Epub 2007 Nov 30.

Abstract

Crotoxin B is a basic phospholipase A2 found in the venom of Crotalus durissus terrificus and is one of the subunits that constitute crotoxin. This heterodimeric toxin, which is the main component of C. d. terrificus venom, is completed by an acidic, nontoxic and non-enzymatic component (crotoxin A) and is involved in important envenomation effects, such as neurological disorders, myotoxicity and renal failure. Although crotoxin was first crystallized in 1938, no crystal structure is currently available for crotoxin, crotoxin A or crotoxin B. In this work, the crystallization, X-ray diffraction data collection to 2.28 A resolution and molecular-replacement solution of a novel tetrameric complex formed by two dimers of crotoxin B isoforms (CB1 and CB2) is presented.

摘要

响尾蛇毒素B是一种碱性磷脂酶A2,存在于南美巨蝮的毒液中,是构成响尾蛇毒素的亚基之一。这种异二聚体毒素是南美巨蝮毒液的主要成分,由一种酸性、无毒且无酶活性的成分(响尾蛇毒素A)与之结合而成,并参与重要的中毒效应,如神经紊乱、肌毒性和肾衰竭。尽管响尾蛇毒素于1938年首次结晶,但目前尚无响尾蛇毒素、响尾蛇毒素A或响尾蛇毒素B的晶体结构。在这项工作中,我们展示了由响尾蛇毒素B亚型(CB1和CB2)的两个二聚体形成的新型四聚体复合物的结晶、分辨率为2.28 Å的X射线衍射数据收集以及分子置换解决方案。

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Crystallization and preliminary X-ray diffraction analysis of crotoxin B from Crotalus durissus collilineatus venom.矛头蝮蛇毒中响尾蛇毒素B的结晶及初步X射线衍射分析
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Oct 1;65(Pt 10):1011-3. doi: 10.1107/S1744309109032631. Epub 2009 Sep 23.

本文引用的文献

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Inference of macromolecular assemblies from crystalline state.从晶体状态推断大分子组装体
J Mol Biol. 2007 Sep 21;372(3):774-97. doi: 10.1016/j.jmb.2007.05.022. Epub 2007 May 13.

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