Construction of a fused grid-based CYP2C18-Template system and its application to drug metabolism

• Published in: Drug metabolism and pharmacokinetics 2024-02, Vol.54, p.100534-100534, Article 100534
• Main Authors: Yamazoe, Yasushi, Yoshinari, Kouichi
• Format: Article
• Language: English
• Subjects: CYP2C18-Mediated metabolism; Fused-grid template; Modes of inhibition; Poor and good substrates; Simulation of ligand-interaction on template
• ISSN: 1347-4367; 1880-0920
• DOI: 10.1016/j.dmpk.2023.100534

Detailed estimation of cytochrome P450 (CYP)-mediated metabolisms of medicine and other chemicals is necessary for the efficacy and safety assessments. Data on the metabolisms mediated by minor CYP enzymes like CYP2C18 are often not available in metabolisms and safety assessments of chemicals except for medical drugs developed recently. A ligand-accessible space in the active site of human CYP2C18 was thus reconstituted as a fused grid-based Template with the use of structural data of its ligands. An evaluation system of CYP2C18-mediated metabolism was then developed on Template with the introduction of the idea of movement and fastening of ligands after Trigger-residue contact. Reciprocal comparison of the data of simulations on Template with experimental results suggested a unified way of the interaction of CYP2C18, in similar to the CYP2C8 interaction (Drug Metab Pharmacokinet 2023, in press). These experiments also displayed the roles of initial Trigger-residue-localizations on their distinct catalyses among human CYP2C enzymes. Simulation experiments for over 130 reactions of CYP2C18 ligands supported the system established.