Insecticide binding to voltage-gated sodium channels
O’Reilly, Andrias O. and Davies, T.G.E. and Usherwood, P.N.R. and Mellor, I. and Williamson, M.S. and Field, L.M. and Wallace, Bonnie A. (2009) Insecticide binding to voltage-gated sodium channels. Biophysical Journal 96 (3(S1)), 14a-14a. ISSN 0006-3495.
Abstract
DDT and the pyrethroid class of insecticides target voltage-gated sodium channels. Their binding stabilises the channel open state, inducing prolonged tail currents associated with insect paralysis (‘knockdown’) and death. Target-site mutations conferring resistance, while a challenge for pest control programs, have provided valuable information on the location of the elusive insecticide-binding site. Homology modelling of the housefly sodium channel and automated ligand docking studies have identified a binding site consistent with resistance-associated mutagenesis data, structure-activity relationships of insecticides and their state-dependent binding activity [O'Reilly et al (2006) Biochem. J. 396:255-263]. The putative binding site, delimited by the domain II S4-S5 linker, S5 & S6 helices and domain III S6 helix, interfaces the lipid bilayer and is therefore accessible to lipid-soluble insecticide ligands. The model is supported by recent experimental results from voltage-clamp electrophysiology studies on mutant fruitfly sodium channels [Usherwood et al (2007) FEBS Letters 581:5485-5492]. The mutation T929I, predicted to inhibit DDT binding through steric hindrance, abolishes the effects of DDT on channel activity. M918, a residue predicted to form a binding contact with pyrethroids but not DDT, decreased deltamethrin potency without effecting DDT potency when mutated. We have developed methods based on circular dichroism spectroscopy to identify ligand binding to a non-insect channel system, namely the voltage-gated sodium channel NaChBac from Bacillus halodurans [Nurani et al (2008) Biochemistry 31:8114-8121], which will be used as a further test of the binding of various insecticides as predicted by the model. (Supported by grants from the BBSRC)
Metadata
Item Type: | Article |
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School: | Birkbeck Faculties and Schools > Faculty of Science > School of Natural Sciences |
Research Centres and Institutes: | Bioinformatics, Bloomsbury Centre for (Closed), Structural Molecular Biology, Institute of (ISMB) |
Depositing User: | Administrator |
Date Deposited: | 04 Aug 2010 14:09 |
Last Modified: | 02 Aug 2023 16:49 |
URI: | https://eprints.bbk.ac.uk/id/eprint/1199 |
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