Interactions of 2-phenyl-benzotriazole xenobiotic compounds with human Cytochrome P450-CYP1A1 by means of docking, molecular dynamics simulations and MM-GBSA calculations. (June 2018)

• Record Type: Journal Article
• Authors: Mena-Ulecia, Karel; MacLeod-Carey, Desmond
• Is Part Of: Computational biology and chemistry. Volume 74(2018)
• Page Start: 253
• Page End: 262
• Publication Date: 2018-06
• Subjects: 2-Phenyl-benzotriazole -- Molecular docking -- Molecular dynamics simulations -- MM-GBSA; Chemistry -- Data processing -- Periodicals; Biology -- Data processing -- Periodicals; Biochemistry -- Data processing; Biology -- Data processing; Molecular biology -- Data processing; Periodicals; Electronic journals; 542.85
• DOI: 10.1016/j.compbiolchem.2018.04.004
• Languages: English
• ISSNs: 1476-9271

Abstract

Graphical abstract: Highlights: Molecular docking analyses reproduce binding modes of 2-phenil-benzotriazoles pro-mutagens with human Cytochrome P450-CYP1A1 within 1, 5 Å of RMSD. MD simulations show that terminal NH2 of PBTAs and triazole group establish π-π interactions and hydrogen bonds with CYP1A1. MM-GBSA binding energy results agree with experimental metabolic activation that PBTA-4 is the highest pro-mutagen compound. Modification of the NH2 over the phenyl group on PBTAs generate subtle changes in the interaction between PBTAs and CYP1A1 . Abstract: 2-phenyl-benzotriazole xenobiotic compounds (PBTA-4, PBTA-6, PBTA-7 and PBTA-8 ) that were previously isolated and identified in waters of the Yodo river, in Japan (Nukaya et al., 2001 ; Ohe et al., 2004 ; Watanabe et al., 2001 ) were characterized as powerful pro-mutagens. In order to predict the activation mechanism of these pro-mutagens, we designed a computational biochemistry protocol, which includes, docking experiments, molecular dynamics simulations and free energy decomposition calculations to obtain information about the interaction of 2-phenyl-benzotriazole molecules into the active center of cytochrome P450-CYP1A1 (CYP1A1 ). Molecular docking calculations using AutoDock Vina software shows that PBTAs are proportionally oriented in the pocket of CYP1A1, establishing π-π stacking attractive interactions between the triazole group and the Phe224, as well as, the hydrogen bonds of the terminal NH2 over the benzotriazole units with the Asn255 and Ser116 amino acids. Molecular dynamics simulations using NAMD package showed that these interactions are stable along 100.0 ns of trajectories. Into this context, free binding energy calculations employing the MM-GBSA approach, shows that some differences exists among the interaction of PBTAs with CYP1A1, regarding the solvation, electrostatic and van der Waals interaction energy components. These results suggest that PBTA molecules might be activated by CYP1A1 . Thus, enhancing their mutagenicity when compared with the pro-mutagen parent species.