Homology modelling of the Apis mellifera nicotinic acetylcholine receptor (nAChR) and docking of imidacloprid and fipronil insecticides and their metabolites

• Published in: SAR and QSAR in environmental research 2008-04, Vol.19 (3-4), p.245-261
• Main Authors: Rocher, A., Marchand-Geneste, N.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Apis mellifera; Bees; Binding Sites; Cholinergic Agents - chemistry; Cholinergic Agents - metabolism; docking; fipronil; homology modelling; imidacloprid; Imidazoles - chemistry; Imidazoles - metabolism; Insecta; Insecticides - chemistry; Insecticides - metabolism; Models, Molecular; Molecular Sequence Data; Neonicotinoids; nicotinic acetylcholine receptor; Nitro Compounds - chemistry; Nitro Compounds - metabolism; Protein Conformation; Pyrazoles - chemistry; Pyrazoles - metabolism; QSAR; Receptors, Nicotinic - chemistry; Receptors, Nicotinic - metabolism; Sequence Alignment; Species Specificity
• ISSN: 1062-936X; 1029-046X
• DOI: 10.1080/10629360802083731

Five homology models for honeybee (Apis mellifera) nicotinic acetylcholine receptor (nAChR) α1/β1, α3/β2, α4/β2, α6/β2 and α9/α9 subtypes were built from the Torpedo marmorata nAChR X-ray structure. Then, imidacloprid, fipronil and their metabolites were docked into the ligand binding domain (LBD) of these receptors and the corresponding scoring functions were calculated. The binding modes of the docked compounds were carefully analysed. Finally, multivariate analyses were used for deriving structure-activity relationships based on hydrogen bond number and scoring functions between the insecticides and the nAChR models.