Use of density functional theory in drug metabolism studies

Research output: Contribution to journalJournal articleResearchpeer-review

Patrik Rydberg, Flemming Steen Jørgensen, Lars Olsen

INTRODUCTION: The cytochrome P450 enzymes (CYPs) metabolize many drug compounds. They catalyze a wide variety of reactions, and potentially, a large number of different metabolites can be generated. Density functional theory (DFT) has, over the past decade, been shown to be a powerful tool to rationalize and predict the possible metabolites generated by the CYPs as well as other drug-metabolizing enzymes.

AREAS COVERED: We review applications of DFT on reactions performed by the CYPs and other drug-metabolizing enzymes able to perform oxidation reactions, with an emphasis on predicting which metabolites are produced. We also cover calculations of binding energies for complexes in which the ligands interact directly with the heme iron atom.

EXPERT OPINION: DFT is a useful tool for prediction of the site of metabolism. The use of small models of the enzymes work surprisingly well for most CYP isoforms. This is probably due to the fact that the binding of the substrates is not the major determinant. When binding of the substrate plays a significant role, the well-known issue of determining the free energy of binding is the challenge. How approaches taking the protein environment into account, like docking, MD and QM/MM, can be used are discussed.

Original languageEnglish
JournalExpert Opinion on Drug Metabolism & Toxicology
Volume10
Issue number2
Pages (from-to)215-27
Number of pages13
ISSN1742-5255
DOIs
Publication statusPublished - Feb 2014

ID: 122540630