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台湾眼镜蛇毒中眼镜蛇毒素的去折叠/折叠研究:pH值和谷胱甘肽/氧化型谷胱甘肽调控C端的二硫键异构化

Unfolding/folding studies on cobrotoxin from Taiwan cobra venom: pH and GSH/GSSG govern disulfide isomerization at the C-terminus.

作者信息

Chang L S, Lin S R, Chang C C

机构信息

Department of Biochemistry, Kaohsiung Medical College, Taiwan, Republic of China.

出版信息

Arch Biochem Biophys. 1998 Jun 1;354(1):1-8. doi: 10.1006/abbi.1998.0660.

Abstract

Refolding of cobrotoxin was assessed by the exposure degree of its single Trp determined by an acrylamide quenching study. The change in the accessibility of Trp for acrylamide quantitatively reflected the formation of folded cobrotoxin, and the data were confirmed by HPLC and gel electrophoresis analyses. However, the site-specific information provided by quenching Trp fluorescence revealed that the ordered structure in the neighborhood of Trp was attained prior to the complete formation of the tertiary structure of cobrotoxin. HPLC analyses showed that, in addition to refolded cobrotoxin, two novel species (cobrotoxin II and cobrotoxin III) with isomerization of disulfide bonds at the C-terminus of the toxin molecule were produced along the folding reaction. The disulfide pairings in cobrotoxin II and cobrotoxin III were Cys43-Cys55 and Cys54-Cys60 and Cys43-Cys60 and Cys54-Cys55, respectively. Among the three possible two-disulfide species at the C-terminus, the disulfide linkages Cys43-Cys60 and Cys54-Cys55 of cobrotoxin III caused a marked decrease in lethality and resulted in a conformation which was notably different from that observed with the native toxin molecule as evidenced by CD spectra. The refolding reaction was accelerated by the addition of GSH/GSSG, and the resulting products were mostly folded cobrotoxin. However, if GSH/GSSG was not added into the initial folding materials, the yields of cobrotoxin II and cobrotoxin III greatly increased. The conversion of cobrotoxin to its isomers was to be irreversible and pH-dependent: the higher the pH, the faster the rate of conversion. However, this conversion could be partly inhibited by GSH/GSSG. Cobrotoxin II and cobrotoxin III were purified from Taiwan cobra venom as well, and their yields in comparison to that of cobrotoxin in venom were similar to that noted with the folded products in the presence of GSH/GSSG. Moreover, the rate of disulfide isomerization was expected to be slow in venom fluid in which the pH was approximately pH 6.2. Thus, the finding that cobrotoxin represents the predominant neurotoxin species in Taiwan cobra venom is probably associated with the synergistic effects of GSH/GSSG and pH.

摘要

通过丙烯酰胺猝灭研究测定的单一色氨酸的暴露程度来评估眼镜蛇毒素的重折叠。色氨酸对丙烯酰胺可及性的变化定量反映了折叠型眼镜蛇毒素的形成,并且该数据通过高效液相色谱(HPLC)和凝胶电泳分析得到证实。然而,猝灭色氨酸荧光所提供的位点特异性信息表明,在眼镜蛇毒素三级结构完全形成之前,色氨酸附近的有序结构就已形成。HPLC分析表明,除了重折叠的眼镜蛇毒素外,在折叠反应过程中还产生了两种新的物种(眼镜蛇毒素II和眼镜蛇毒素III),它们在毒素分子的C端具有二硫键异构化。眼镜蛇毒素II和眼镜蛇毒素III中的二硫键配对分别是Cys43-Cys55和Cys54-Cys60以及Cys43-Cys60和Cys54-Cys55。在C端三种可能的双二硫键物种中,眼镜蛇毒素III的二硫键连接Cys43-Cys60和Cys54-Cys55导致致死率显著降低,并导致一种构象,该构象与天然毒素分子观察到的构象明显不同,圆二色光谱(CD光谱)证明了这一点。通过添加还原型谷胱甘肽/氧化型谷胱甘肽(GSH/GSSG)可加速重折叠反应,并且所得产物大多为重折叠的眼镜蛇毒素。然而,如果在初始折叠材料中不添加GSH/GSSG,眼镜蛇毒素II和眼镜蛇毒素III的产量会大大增加。眼镜蛇毒素向其异构体的转化是不可逆的且依赖于pH值:pH值越高,转化速率越快。然而,这种转化可被GSH/GSSG部分抑制。眼镜蛇毒素II和眼镜蛇毒素III也从台湾眼镜蛇毒液中纯化得到,与毒液中眼镜蛇毒素的产量相比,它们的产量与在存在GSH/GSSG时折叠产物的产量相似。此外,在pH约为6.2的毒液中,二硫键异构化速率预计较慢。因此,眼镜蛇毒素是台湾眼镜蛇毒液中主要神经毒素物种这一发现可能与GSH/GSSG和pH的协同作用有关。

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