Enzyme-catalyzed side reactions with molecular oxygen may contribute to cell signaling and neurodegenerative diseases

被引:37
作者
Bunik, Victoria I.
Schloss, John V.
Pinto, John T.
Gibson, Gary E.
Cooper, Arthur J. L.
机构
[1] Cornell Univ, Coll Med, Burke Med Res Inst, White Plains, NY 10605 USA
[2] Moscow MV Lomonosov State Univ, Sch Bioengn & Bioinformat, Moscow 119992, Russia
[3] Moscow MV Lomonosov State Univ, Belozersky Inst Phys Chem Biol, Moscow 119992, Russia
[4] NeuroSystec, Valencia, CA 91355 USA
[5] Cornell Univ, Weill Med Coll, Dept Neurol & Neurosci, New York, NY 10021 USA
[6] Cornell Univ, Weill Med Coll, Dept Biochem, New York, NY 10021 USA
关键词
branched chain alpha-keto acid dehydrogenase complex; carbanion intermediates; alpha-ketoglutarate dehydrogenase complex; pyridoxal 5'-phosphate; pyruvate dehydrogenase complex; thiamine diphosphate;
D O I
10.1007/s11064-006-9239-z
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 link between neurodegeneration and well-characterized enzymatic and non-enzymatic reactions that produce reactive oxygen species (ROS) from O-2 is well established. Several enzymes that contain pyridoxal 5'-phosphate (PLP) or thiamine diphosphate (ThDP) catalyze side reactions (paracatalytic reactions) in the presence of ambient O-2. These side reactions produce oxidants such as hydrogen peroxide [H2O2] or extremely reactive peracids [RC(O)OOH]. We hypothesize that although these enzymes normally produce oxidants at low or undetectable levels, changes in substrate levels or disease-induced structural alterations may enhance interactions with O-2, thereby generating higher levels of reactive oxidants. These oxidants may damage the enzymes producing them, alter nearby macromolecules and/or destroy important metabolites/coenzymes. We propose that paracatalytic reactions with O-2 catalyzed by PLP-dependent decarboxylases and by ThDP-dependent enzymes within the alpha-keto acid dehydrogenase complexes may contribute to normal cellular signaling and to cellular damage in neurodegenerative diseases.
引用
收藏
页码:871 / 891
页数:21
相关论文
共 130 条
[91]  
LUCIGNANI G, 1993, J NUCL MED, V34, P360
[92]   Immunochemical identification of coenzyme Q0-dihydrolipoamide adducts in the E2 components of the α-ketoglutarate and pyruvate dehydrogenase complexes partially explains the cellular toxicity of coenzyme Q0 [J].
MacDonald, MJ ;
Husain, RD ;
Hoffmann-Benning, S ;
Baker, TR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (26) :27278-27285
[93]   A versatile conformational switch regulates reactivity in human branched-chain α-ketoacid dehydrogenase [J].
Machius, M ;
Wynn, RM ;
Chuang, JL ;
Li, J ;
Kluger, R ;
Yu, D ;
Tomchick, DR ;
Brautigam, CA ;
Chuang, DT .
STRUCTURE, 2006, 14 (02) :287-298
[94]  
Markiewicz J, 1997, BIOCHEM ARCH, V13, P127
[95]  
MASSEY V, 1969, J BIOL CHEM, V244, P3999
[96]   Carbamoylation of brain glutamate receptors by a disulfiram metabolite [J].
Nagendra, SN ;
Faiman, MD ;
Davis, K ;
Wu, JY ;
Newby, X ;
Schloss, JV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) :24247-24251
[97]   Metabolic impairment induces oxidative stress, compromises inflammatory responses, and inactivates a key mitochondrial enzyme in microglia [J].
Park, LCH ;
Zhang, H ;
Sheu, KFR ;
Calingasan, NY ;
Kristal, BS ;
Lindsay, JG ;
Gibson, GE .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (05) :1948-1958
[98]   RAPID INACTIVATION OF BRAIN GLUTAMATE-DECARBOXYLASE BY ASPARTATE [J].
PORTER, TG ;
MARTIN, DL .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (01) :67-72
[99]   Are mitochondria critical in the pathogenesis of Alzheimer's disease? [J].
Reddy, PH ;
Beal, MF .
BRAIN RESEARCH REVIEWS, 2005, 49 (03) :618-632
[100]   INFLUENCE OF COMPLETE AND PRONOUNCED INCOMPLETE CEREBRAL-ISCHEMIA AND SUBSEQUENT RECIRCULATION ON CORTICAL CONCENTRATIONS OF OXIDIZED AND REDUCED GLUTATHIONE IN THE RAT [J].
REHNCRONA, S ;
FOLBERGROVA, J ;
SMITH, DS ;
SIESJO, BK .
JOURNAL OF NEUROCHEMISTRY, 1980, 34 (03) :477-486