An assessment of the reaction energetics for cytochrome P450-mediated reactions

被引:36
作者
Higgins, L
Korzekwa, KR
Rao, S
Shou, MG
Jones, JP
机构
[1] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[2] Univ Washington, Dept Med Chem, Seattle, WA 98195 USA
[3] Camitro Corp, Menlo Park, CA 94025 USA
[4] Merck Res Labs, Dept Drug Metab, W Point, PA 19486 USA
关键词
D O I
10.1006/abbi.2000.2147
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
Regioselectivity is used to determine the absolute energetic differences for four different reactions catalyzed by P450, Abstraction of a hydrogen from a benzylic carbon containing a chlorine has a 1.0 kcal/mol lower barrier than abstraction from a simple benzylic carbon, which in turn is 0.4 to 0.9 kcal/mol lower than abstraction from the methyl group of an aromatic ether and 0.1 to 0.6 kcal/mol easier than aromatic hydroxylation. Isotope effects are used to determine if the enzyme-substrate complexes leading to each product, from a given substrate, are in rapid equilibrium, For all enzymes isotopically sensitive branching is observed from the benzylic carbon upon deuterium incorporation at that position to each of the other positions, indicating that each product arises from the same active oxygen species. The energetic differences determined experimentally are accurately reproduced by theoretical hydrogen atom abstractions at both the AM1 semiempirical and DFT levels of theory. (C) 2001 Academic Press.
引用
收藏
页码:220 / 230
页数:11
相关论文
共 40 条
[1]   Experimental and theoretical study of the effect of active-site constrained substrate motion on the magnitude of the observed intramolecular isotope effect for the P450 101 catalyzed benzylic hydroxylation of isomeric xylenes and 4,4′-dimethylbiphenyl [J].
Audergon, C ;
Iyer, KR ;
Jones, JP ;
Darbyshire, JF ;
Trager, WF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (01) :41-47
[2]   VALPROIC ACID METABOLISM BY CYTOCHROME-P450 - A THEORETICAL-STUDY OF STEREOELECTRONIC MODULATORS OF PRODUCT DISTRIBUTION [J].
COLLINS, JR ;
CAMPER, DL ;
LOEW, GH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (07) :2736-2743
[3]  
COLLINS JR, 1988, J BIOL CHEM, V263, P3164
[4]  
DEMONTELLANO PRO, 1991, J AM CHEM SOC, V113, P3195
[5]   ON ISOTOPE EFFECTS FOR THE CYTOCHROME-P-450 OXIDATION OF SUBSTITUTED N,N-DIMETHYLANILINES [J].
DINNOCENZO, JP ;
KARKI, SB ;
JONES, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (16) :7111-7116
[6]  
Ekins S, 1999, J PHARMACOL EXP THER, V288, P21
[7]   ETHYLBENZENE HYDROXYLATION BY CYTOCHROME-P450CAM [J].
FILIPOVIC, D ;
PAULSEN, MD ;
LOIDA, PJ ;
SLIGAR, SG ;
ORNSTEIN, RL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 189 (01) :488-495
[8]   Positional specificity of rabbit CYP4B1 for ω-hydroxylation of short-medium chain fatty acids and hydrocarbons [J].
Fisher, MB ;
Zheng, YM ;
Rettie, AE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (02) :352-355
[9]   THIOANISOLE SULFOXIDATION BY CYTOCHROME P450(CAM) (CYP101) - EXPERIMENTAL AND CALCULATED ABSOLUTE STEREOCHEMISTRIES [J].
FRUETEL, J ;
CHANG, YT ;
COLLINS, J ;
LOEW, G ;
DEMONTELLANO, PRO .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (26) :11643-11648
[10]   MODELING CYANIDE RELEASE FROM NITRILES - PREDICTION OF CYTOCHROME P450 MEDIATED ACUTE NITRILE TOXICITY [J].
GROGAN, J ;
DEVITO, SC ;
PEARLMAN, RS ;
KORZEKWA, KR .
CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (04) :548-552