Ajoene is an inhibitor and subversive substrate of human glutathione reductase and Trypanosoma cruzi trypanothione reductase:: Crystallographic, kinetic, and spectroscopic studies

被引:88
作者
Gallwitz, H
Bonse, S
Martinez-Cruz, A
Schlichting, I
Schumacher, K
Krauth-Siegel, RL
机构
[1] Heidelberg Univ, Zentrum Biochem, D-69120 Heidelberg, Germany
[2] Max Planck Inst Med Res, Biophys Abt, D-69120 Heidelberg, Germany
[3] Max Planck Inst Mol Physiol, D-44139 Dortmund, Germany
[4] Gesell Biotechnol Forsch mbH, D-38124 Braunschweig, Germany
关键词
D O I
10.1021/jm980471k
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ajoene ((E,Z)-4,5,9-trithiadodeca-1,6,11-triene 9-oxide), a garlic-derived natural compound, is a covalent; inhibitor as well as a substrate of human glutathione reductase (GR) and Trypanosoma cruzi trypanothione reductase (TR). The 2.1-Angstrom resolution crystal structure of GR inhibited by (E)-ajoene revealed a mixed disulfide between the active site Cys58 and the CH2=CH-CH2-SO-CH2-CH=CH-S moiety of ajoene. The modified enzyme has a markedly increased oxidase activity when compared to free GR, GR reduces (Z)-ajoene with a k(cat)/K-m of 6.8 x 10(3) M-1 s(-1) yielding 4,5,9-trithiadodeca-1,6,11-triene (deoxyajoene) and 4,8,9,13-tetrathiahexadeca-1,6,10,15-tetraene as stable reaction products. The reaction leads also to the formation of single-electron reduced products and concomitantly superoxide anion radicals as shown by coupling the reaction to the reduction of cytochrome c. The interactions between the flavoenzymes and ajoene are expected to increase the oxidative stress of the respective cell. The antiparasitic and cytostatic actions of ajoene may at least in part be due to the multiple effects on key enzymes of the antioxidant thiol metabolism.
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页码:364 / 372
页数:9
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