Department of Medicinal Chemistry, University of Washington, Seattle, WA 98195-7610, USA.
Arch Biochem Biophys. 2011 Mar 1;507(1):56-65. doi: 10.1016/j.abb.2010.10.006. Epub 2010 Oct 19.
Cytochrome P450s (CYPs) are heme-containing monooxygenases that contribute to an enormous range of enzymatic function including biosynthetic and detoxification roles. This review summarizes recent studies concerning interactions of CYPs with ligands including substrates, inhibitors, and diatomic heme-ligating molecules. These studies highlight the complexity in the relationship between the heme spin state and active site occupancy, the roles of water in directing protein-ligand and ligand-heme interactions, and the details of interactions between heme and gaseous diatomic CYP ligands. Both kinetic and thermodynamic aspects of ligand binding are considered.
细胞色素 P450 酶(CYPs)是一类含有血红素的单加氧酶,参与了广泛的酶学功能,包括生物合成和解毒作用。本文综述了最近关于 CYPs 与配体相互作用的研究,包括底物、抑制剂和双原子血红素配体分子。这些研究强调了血红素自旋状态与活性位点占据之间关系的复杂性、水在指导蛋白-配体和配体-血红素相互作用中的作用,以及血红素与气态双原子 CYP 配体相互作用的细节。同时考虑了配体结合的动力学和热力学方面。