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细胞色素P450催化作用中的限速步骤。

Rate-limiting steps in cytochrome P450 catalysis.

作者信息

Guengerich F Peter

出版信息

Biol Chem. 2002 Oct;383(10):1553-64. doi: 10.1515/BC.2002.175.

Abstract

Cytochrome P450 (P450) reactions are of interest because of their relevance to the oxidative metabolism of drugs, steroids, carcinogens, and other chemicals. One of the considerations about functional characterization is which steps of the catalytic cycle are rate-limiting. Detailed analysis indicates that several different steps can be rate-limiting with individual P450 reactions. N-Dealkylation of para-substituted N,N-dimethylanilines is a function of the electron withdrawing/donating properties of the substituent and the oxidation-reduction potential of the substrate, supporting a role in rate-limiting electron transfer from substrate to the high valent P450. In the oxidations of ethanol and acetaldehyde by human P450 2E1, a step following product formation must be the slow step (but not product release per se). Several oxidations catalyzed by human P450s 1A2 and 2D6 show slow C-H bond breaking, and apparent high-valent iron complexes accumulate in the reaction steady-state. Kinetic simulations were used to test the suitability of potential schemes and to probe the effects of changes in individual reaction steps.

摘要

细胞色素P450(P450)反应因其与药物、类固醇、致癌物及其他化学物质的氧化代谢相关而备受关注。功能表征方面的一个考量是催化循环的哪些步骤是限速步骤。详细分析表明,个别P450反应中几个不同的步骤都可能是限速步骤。对位取代的N,N - 二甲基苯胺的N - 脱烷基化反应取决于取代基的吸电子/供电子性质以及底物的氧化还原电位,这支持了从底物到高价P450的限速电子转移作用。在人P450 2E1催化乙醇和乙醛的氧化反应中,产物形成后的一个步骤必定是慢步骤(但不是产物本身的释放)。人P450 1A2和2D6催化的几种氧化反应显示出缓慢的C - H键断裂,并且在反应稳态中会积累明显的高价铁配合物。动力学模拟用于测试潜在方案的适用性,并探究各个反应步骤变化的影响。

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