Mechanism of copper-catalyzed oxidation of glutathione

被引:128
作者
Kachur, AV [1 ]
Koch, CJ [1 ]
Biaglow, JE [1 ]
机构
[1] Univ Penn, Sch Med, Dept Radiat Oncol, Philadelphia, PA 19104 USA
关键词
glutathione; oxidation; copper; hydroxyl radical; superoxide radical; hydrogen peroxide;
D O I
10.3109/10715769809069278
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
The mechanism of copper-catalyzed glutathione oxidation was investigated using oxygen consumption, thiol depletion, spectroscopy and hydroxyl radical detection. The mechanism of oxidation has kinetics which appear biphasic. During the first reaction phase a stoichiometric amount of oxygen is consumed (1 mole oxygen per 4 moles thiol) with minimal (OH)-O-. production. In the second reaction phase, additional (excess) oxygen is consumed at an increased rate and with significant hydrogen peroxide and (OH)-O-. production. The kinetic and spectroscopic data suggest that copper forms a catalytic complex with glutathione (1 mole copper per 2 moles glutathione). Our proposed reaction mechanism assumes two parallel processes (superoxide-dependent and peroxide-dependent) for the first reaction phase and superoxide-independent for the second phase. Our current results indicate that glutathione, usually considered as an antioxidant, can act as prooxidant at physiological conditions and therefore can participate in cellular radical damage.
引用
收藏
页码:259 / 269
页数:11
相关论文
共 26 条
[1]   GENERATION OF HYDROGEN-PEROXIDE BY INCIDENTAL METAL ION-CATALYZED AUTOOXIDATION OF GLUTATHIONE [J].
ALBRO, PW ;
CORBETT, JT ;
SCHROEDER, JL .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1986, 27 (03) :191-203
[2]   FACTORS INFLUENCING THE OXIDATION OF CYSTEAMINE AND OTHER THIOLS - IMPLICATIONS FOR HYPERTHERMIC SENSITIZATION AND RADIATION PROTECTION [J].
BIAGLOW, JE ;
ISSELS, RW ;
GERWECK, LE ;
VARNES, ME ;
JACOBSON, B ;
MITCHELL, JB ;
RUSSO, A .
RADIATION RESEARCH, 1984, 100 (02) :298-312
[3]   The generation of hydroxyl radicals in the reaction of molecular oxygen with polyphosphate complexes of ferrous ion [J].
Biaglow, JE ;
Kachur, AV .
RADIATION RESEARCH, 1997, 148 (02) :181-187
[4]   EFFECTS OF N-ACETYLCYSTEINE IN THE RAT-HEART REPERFUSED AFTER LOW-FLOW ISCHEMIA - EVIDENCE FOR A DIRECT SCAVENGING OF HYDROXYL RADICALS AND A NITRIC OXIDE-DEPENDENT INCREASE IN CORONARY FLOW [J].
BRUNET, J ;
BOILY, MJ ;
CORDEAU, S ;
DESROSIERS, C .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 19 (05) :627-638
[5]   THE PECKING ORDER OF FREE-RADICALS AND ANTIOXIDANTS - LIPID-PEROXIDATION, ALPHA-TOCOPHEROL, AND ASCORBATE [J].
BUETTNER, GR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (02) :535-543
[6]   COPPER CATALYZED OXIDATION OF CYSTEINE TO CYSTINE [J].
CAVALLINI, D ;
DEMARCO, C ;
DUPRE, S ;
ROTILIO, G .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1969, 130 (1-2) :354-+
[7]   Loss of GSH, oxidative stress, and decrease of intracellular pH as sequential steps in viral infection [J].
Ciriolo, MR ;
Palamara, AT ;
Incerpi, S ;
Lafavia, E ;
Bue, MC ;
DeVito, P ;
Garaci, E ;
Rotilio, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (05) :2700-2708
[8]   COUMARIN CHEMICAL DOSIMETER FOR RADIATION-THERAPY [J].
COLLINS, AK ;
MAKRIGIORGOS, GM ;
SVENSSON, GK .
MEDICAL PHYSICS, 1994, 21 (11) :1741-1747
[9]   COPPER(I) TRANSFER INTO METALLOTHIONEIN MEDIATED BY GLUTATHIONE [J].
FERREIRA, AMD ;
CIRIOLO, MR ;
MARCOCCI, L ;
ROTILIO, G .
BIOCHEMICAL JOURNAL, 1993, 292 :673-676
[10]   INTRACELLULAR COPPER TRANSPORT IN CULTURED HEPATOMA-CELLS [J].
FREEDMAN, JH ;
PEISACH, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 164 (01) :134-140