Oxidation of tetrahydrobiopterin by peroxynitrite or oxoferryl species occurs by a radical pathway

被引:31
作者
Kohnen, SL
Mouithys-Mickalad, AA
Deby-Dupont, GP
Deby, CMT
Lamy, ML
Noels, AF
机构
[1] Univ Liege, Ctr Oxygen Res & Dev, Inst Chim, B-4000 Liege, Belgium
[2] Univ Liege, CERM, Lab Homogeneous Catalysis, Inst Chim, B-4000 Liege, Belgium
[3] Univ Liege, Ctr Hosp Univ, Dept Anaesthesia & Intens Care, B-4000 Liege, Belgium
关键词
tetrahydrobiopterin; peroxynitrite; oxoferryl; chemiluminescence; electron paramagnetic resonance; diode array spectrophotometry;
D O I
10.1080/10715760100301221
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 molecular mechanisms of tetrahydrobiopterin (BH4) oxidation by peroxynitrite (ONCO-) was studied using ultra-weak chemiluminescence, electron paramagnetic resonance (EPR) and UV-visible diode-array spectrophotometry, and compared to BH4 oxidation by oxoferryl species produced by the myoglobin/hydrogen peroxide (Mb/H2O2) system. The oxidation of BH4 by ONOO- produced a weak chemiluminescence, which was altered by addition of 50mM of the spin trap alpha-(4-pyridyl-1-oxide)-N-tert butylnitrone (POBN). EPR spin trapping demonstrated that the reaction occurred at least in part by a radical pathway. A mixture of two spectra composed by an intense six-line spectrum and a fleeting weak nine-line one was observed when using ONOO-. Mb/H2O2 produced a short-living light emission that was suppressed by the addition of BH4. Simultaneous addition of POBN, BH4 and Mb/H2O2 produced the same six-line EPR spectrum, with a signal intensity depending on BH4 concentration. Spectrophotometric studies confirmed the rapid disappearance of the characteristic peak of ONOO- (302nm) as well as substantial modifications of the initial BH4 spectrum with both oxidant systems. These data demonstrated that BH4 oxidation, either by ONOO- or by Mb/H2O2, occurred with the production of activated species and by radical pathways.
引用
收藏
页码:709 / 721
页数:13
相关论文
共 45 条
  • [1] Peroxynitrite-dependent tryptophan nitration
    Alvarez, B
    Rubbo, H
    Kirk, M
    Barnes, S
    Freeman, BA
    Radi, R
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (02) : 390 - 396
  • [2] THE KINETICS OF THE OXIDATION OF L-ASCORBIC-ACID BY PEROXYNITRITE
    BARTLETT, D
    CHURCH, DF
    BOUNDS, PL
    KOPPENOL, WH
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (01) : 85 - 92
  • [3] KINETICS AND MECHANISM OF AUTOXIDATION OF 2-AMINO-4-HYDROXY-5,6,7,8-TETRAHYDROPTERIDINES
    BLAIR, JA
    PEARSON, AJ
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1974, (01): : 80 - 88
  • [4] Bohle DS, 1996, METHOD ENZYMOL, V269, P302
  • [5] BIOMIMETIC SYNTHESIS OF THE PUTATIVE CYTOTOXIN PEROXYNITRITE, ONOO-, AND ITS CHARACTERISTICS AS A TETRAMETHYLAMMONIUM SALT
    BOHLE, DS
    HANSERT, B
    PAULSON, SC
    SMITH, BD
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (16) : 7423 - 7424
  • [6] Pterin-4α-carbinolamine dehydratase in rat brain I.: Patterns of co-localization with tyrosine hydroxylase
    Depaepe, V
    Cuvelier, L
    Thöny, B
    Résibois, A
    [J]. MOLECULAR BRAIN RESEARCH, 2000, 75 (01): : 76 - 88
  • [7] FISHER DB, 1973, J BIOL CHEM, V248, P4300
  • [8] THE REACTION OF ASCORBIC-ACID WITH DIFFERENT HEME IRON REDOX STATES OF MYOGLOBIN - ANTIOXIDANT AND PROOXIDANT ASPECTS
    GIULIVI, C
    CADENAS, E
    [J]. FEBS LETTERS, 1993, 332 (03) : 287 - 290
  • [9] Reactions of peroxynitrite with gamma-tocopherol
    Hoglen, NC
    Waller, SC
    Sipes, IG
    Liebler, DC
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (04) : 401 - 407
  • [10] THE REACTION OF NO WITH SUPEROXIDE
    HUIE, RE
    PADMAJA, S
    [J]. FREE RADICAL RESEARCH COMMUNICATIONS, 1993, 18 (04): : 195 - 199