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Molecular recognition of thiaclopride by Aplysia californica AChBP: new insights from a computational investigation

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Abstract

The binding of thiaclopride (THI), a neonicotinoid insecticide, with Aplysia californica acetylcholine binding protein (Ac-AChBP), the surrogate of the extracellular domain of insects nicotinic acetylcholine receptors, has been studied with a QM/QM′ hybrid methodology using the ONIOM approach (M06-2X/6-311G(d):PM6). The contributions of Ac-AChBP key residues for THI binding are accurately quantified from a structural and energetic point of view. The importance of water mediated hydrogen-bond (H-bond) interactions involving two water molecules and Tyr55 and Ser189 residues in the vicinity of the THI nitrile group, is specially highlighted. A larger stabilization energy is obtained with the THI–Ac-AChBP complex compared to imidacloprid (IMI), the forerunner of neonicotinoid insecticides. Pairwise interaction energy calculations rationalize this result with, in particular, a significantly more important contribution of the pivotal aromatic residues Trp147 and Tyr188 with THI through CH···π/CH···O and π–π stacking interactions, respectively. These trends are confirmed through a complementary non-covalent interaction (NCI) analysis of selected THI–Ac-AChBP amino acid pairs.

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Acknowledgments

J.Y.L.Q. acknowledges the Région des Pays de la Loire for financial support in the framework of the ECRIN “Paris Scientifiques” Grant. This work was granted access to the HPC resources of [CCRT/CINES/IDRIS] under the allocation c2014085117 made by GENCI (Grand Equipement National de Calcul Intensif). The authors gratefully acknowledge the CCIPL (Centre de Calcul Intensif des Pays de la Loire) for grants of computer time.

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Correspondence to Jean-Yves Le Questel.

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Alamiddine, Z., Selvam, B., Cerón-Carrasco, J.P. et al. Molecular recognition of thiaclopride by Aplysia californica AChBP: new insights from a computational investigation. J Comput Aided Mol Des 29, 1151–1167 (2015). https://doi.org/10.1007/s10822-015-9884-x

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