A bis-cyclodextrin diselenide with glutathione peroxidase-like activity

被引:79
作者
Liu, JQ
Luo, GM [1 ]
Ren, XJ
Mu, Y
Bai, Y
Shen, JC
机构
[1] Jilin Univ, Key Lab Mol Enzymol & Engn, Changchun 130023, Peoples R China
[2] Univ PLA, Changchun 130026, Peoples R China
[3] Jilin Univ, Key Lab Supramol Struct & Spect, Changchun 130023, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 2000年 / 1481卷 / 02期
关键词
beta-cyclodextrin; glutathione peroxidase; imitating enzyme; selenium;
D O I
10.1016/S0167-4838(00)00130-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A diselenide, 2,2'-diseleno-bis-beta-cyclodextrin (2-SeCD), was synthesized to imitate the antioxidant enzyme glutathione peroxidase (GPX). The GPX mimic accepts a variety of hydroperoxides as substrates. The GPX activities, reduction of H2O2, tert-butyl hydroperoxide and cumenyl hydroperoxide by glutathione, are 7.4, 4.5 and 10.2 U/mu mol, respectively. In contrast to ebselen (PZ51), the diselenide displays high GPX-like activity. The reduction of hydroperoxide by glutathione in the presence of a radical trap shows that the mimic catalyzes the reaction via a non-radical mechanism. A ping-pong mechanism was observed in the steady-state kinetic studies of the 2-SeCD-catalyzed reaction. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:222 / 228
页数:7
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