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PMID: 18247580 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Multiple-ligand binding in CYP2A6: probing mechanisms of cytochrome P450 cooperativity by assessing substrate dynamics.

Biochemistry ·Vol. 47 ·No. 9 ·2008-03-04 ·Pages 2978-88

Harrelson JP, Atkins WM, Nelson SD

Abstract

The contribution of ligand dynamics to CYP allosterism has not been considered in detail. On the basis of a previous study, we hypothesized that CYP2A6 and CYP2E1 accommodate multiple xylene ligands. As a result, the intramolecular ( k H/ k D) obs values observed for some xylene isomers are expected to be dependent on ligand concentration with contributions from [CYP.xylene] and [CYP.xylene.xylene], etc. To explore this possibility and the utility of kinetic isotope effects in characterizing allosteric CYP behavior, steady state kinetics, product ratios, and ( k H/ k D) obs values for CYP2E1 and CYP2A6 oxidation of m-xylene-alpha- (2)H 3 and p-xylene-alpha- (2)H 3 were determined. Evidence is presented that CYP2A6 accommodates multiple ligands and that intramolecular isotope effect experiments can provide insight into the mechanisms of multiple-ligand binding. CYP2A6 exhibited cooperative kinetics for m-xylene-alpha- (2)H 3 oxidation and a concentration-dependent decrease in the m-methylbenzylalcohol:2,4-dimethylphenol product ratio (9.8 +/- 0.1 and 4.8 +/- 0.3 at 2.5 microM and 1 mM, respectively). Heterotropic effects were observed as well, as incubations containing both 15 microM m-xylene-alpha- (2)H 3 and 200 microM p-xylene resulted in further reduction of the product ratio (2.4 +/- 0.2). When p-xylene (60 microM) was replaced with deuterium-labeled d 6- p-xylene (60 microM), an intermolecular competitive inverse isotope effect on 2,4-dimethylphenol formation [( k H/ k D) obs = 0.49] was observed, indicating that p-xylene exerts heterotropic effects by residing in the active site simultaneously with m-xylene. The data indicate that there is a concentration-dependent decrease in the reorientation rate of m-xylene, as no increase in ( k H/ k D) obs was observed in the presence of an increased level of metabolic switching. That is, the accommodation of a second xylene molecule in the active site leads to a decrease in substrate dynamics.

MeSH Terms
Algorithms Aryl Hydrocarbon Hydroxylases/metabolism Binding Sites Cytochrome P-450 CYP2A6 Cytochrome P-450 Enzyme System/metabolism Humans Kinesics Kinetics Ligands Mixed Function Oxygenases/metabolism Models, Biological Models, Chemical Molecular Structure Oxidation-Reduction Protein Binding Substrate Specificity Xylenes/chemistry,metabolism
Chemicals
Ligands Xylenes Cytochrome P-450 Enzyme System Mixed Function Oxygenases Aryl Hydrocarbon Hydroxylases CYP2A6 protein, human Cytochrome P-450 CYP2A6
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Harrelson John P
School of Pharmacy, Pacific University, HPC-Ste 451, Hillsboro, Oregon 97123, USA. [email protected]
Atkins William M
Nelson Sidney D
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2008-03-04
Epub
2008-00-05
Pages
2978-88
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM 32165 · United States
NIEHS NIH HHS · P30ES07033 · United States
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