Caffeine Biodegradation by Cytochrome P450 1A2. What Determines the Product Distributions?

被引:23
作者
Mokkawes, Thirakorn [1 ,2 ]
de Visser, Sam P. [1 ,2 ]
机构
[1] Univ Manchester, Manchester Inst Biotechnol, 131 Princess St, Manchester M1 7DN, Lancs, England
[2] Univ Manchester, Dept Chem Engn, Oxford Rd, Manchester M13 9PL, Lancs, England
关键词
density functional theory; enzyme catalysis; heme enzymes; hydroxylation; inorganic reaction mechanisms; MECHANISM-BASED INACTIVATION; MOLECULAR-ORBITAL METHODS; COMPOUND-I; HYDROGEN ABSTRACTION; ELECTRONIC-STRUCTURE; REACTIVITY PATTERNS; REBOUND MECHANISM; DRUG-METABOLISM; AB-INITIO; HYDROXYLATION;
D O I
10.1002/chem.202203875
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Caffeine is a natural compound found in plant seeds that after consumption by humans effects the central nervous system as well as the cardiovascular system. In general, the cytochrome P450 enzymes in the liver are involved in the biodegradation of caffeine, which gives paraxanthine, theobromine and theophylline products. There has been debate for many years why multiple products are obtained and how their distributions are determined. To this end we performed a high-level computational study using a combination of molecular dynamics and quantum mechanical approaches. A series of quantum chemical cluster models on the mechanism of caffeine activation by P450 model complexes give hydrogen atom abstraction barriers that predicts the correct ordering and statistical distribution of products. Our studies highlight that second-coordination sphere effects and thermochemical properties of the substrate determine the product distributions.
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页数:10
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