Binding affinity between AhR and exogenous/endogenous ligands: molecular simulations and biological experiment

Aryl hydrocarbon receptor (AhR) plays critical roles in cell differentiation, and its mechanism is controlled by exogenous and endogenous ligands. However, structures of AhR and its complex with ligand have not been determined by experimental structural biology. We here obtain stable structures of t...

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Bibliographic Details
Published in:	Molecular simulation Vol. 41; no. 7; pp. 555 - 563
Main Authors:	Miyagi, Satoshi, Murata, Kyoshiro, Sashino, Kazuya, Sawamura, Satoshi, Uruno, Saeko, Yoshimura, Seiko, Akahoshi, Eiichi, Ishihara-Sugano, Mitsuko, Itoh, Satoshi, Kurita, Noriyuki
Format:	Journal Article
Language:	English
Published:	Taylor & Francis 03-05-2015
Subjects:	aryl hydrocarbon receptor bioassay endogenous ligand fragment molecular orbital molecular simulation
Online Access:	Get full text
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Summary:	Aryl hydrocarbon receptor (AhR) plays critical roles in cell differentiation, and its mechanism is controlled by exogenous and endogenous ligands. However, structures of AhR and its complex with ligand have not been determined by experimental structural biology. We here obtain stable structures of the complexes with rat AhR (rAhR) and some ligands in water by molecular simulations based on homology modelling, protein-ligand docking, classical molecular mechanics optimisation and ab initio fragment molecular orbital (FMO) calculations. In addition, the binding affinities and the specific interactions between rAhR and the ligands are investigated by ab initio FMO calculations and biological experiments. The experiments reveal the dependence of the rAhR-mediated transcriptional activation on the ligand binding. On the other hand, the results of FMO calculations elucidate that the exogenous ligands interact with many residues of rAhR, while the endogenous ligands interact specifically with a few residues, and that the side chain of Gln381 of rAhR interacts strongly with the oxygen atom located at the centre of the ligand. Furthermore, we evaluate the binding energies between rAhR and the ligands by the FMO method and compare them with the transcriptional activation obtained by the experiment.
ISSN:	0892-7022 1029-0435
DOI:	10.1080/08927022.2014.899696