Evaluation of Atypical Cytochrome P450 Kinetics with Two-Substrate Models:  Evidence That Multiple Substrates Can Simultaneously Bind to Cytochrome P450 Active Sites

• Published in: Biochemistry (Easton) 1998-03, Vol.37 (12), p.4137-4147
• Main Authors: Korzekwa, K. R, Krishnamachary, N, Shou, M, Ogai, A, Parise, R. A, Rettie, A. E, Gonzalez, F. J, Tracy, T. S
• Format: Article
• Language: English
• Subjects: Aryl Hydrocarbon Hydroxylases; Binding Sites; Carbamazepine - metabolism; Cytochrome P-450 CYP2C9; Cytochrome P-450 CYP3A; Cytochrome P-450 Enzyme System - chemistry; Cytochrome P-450 Enzyme System - metabolism; Dapsone - metabolism; Humans; Kinetics; Microsomes, Liver - enzymology; Mixed Function Oxygenases - metabolism; Models, Chemical; Naproxen - metabolism; Protein Binding; Steroid 16-alpha-Hydroxylase; Steroid Hydroxylases - metabolism; Substrate Specificity
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi9715627

Some cytochrome P450 catalyzed reactions show atypical kinetics, and these kinetic processes can be grouped into five categories:  activation, autoactivation, partial inhibition, substrate inhibition, and biphasic saturation curves. A two-site model in which the enzyme can bind two substrate molecules simultaneously is presented which can be used to describe all of these observed kinetic properties. Sigmoidal kinetic characteristics were observed for carbamazepine metabolism by CYP3A4 and naphthalene metabolism by CYPs 2B6, 2C8, 2C9, and 3A5 as well as dapsone metabolism by CYP2C9. Naphthalene metabolism by CYP3A4 and naproxen metabolism by CYP2C9 demonstrated nonhyperbolic enzyme kinetics suggestive of a low K m, low V max component for the first substrate molecule and a high K m, high V max component for the second substrate molecule. 7,8-Benzoflavone activation of phenanthrene metabolism by CYP3A4 and dapsone activation of flurbiprofen and naproxen metabolism by CYP2C9 were also observed. Furthermore, partial inhibition of 7,8-benzoflavone metabolism by phenanthrene was observed. These results demonstrate that various P450 isoforms may exhibit atypical enzyme kinetics depending on the substrate(s) employed and that these results may be explained by a model which includes simultaneous binding of two substrate molecules in the active site.