Journal
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Volume 1862, Issue 10, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.bbamem.2020.183378
Keywords
Fipronil; Gabaergic insecticides; Langmuir monolayers; Molecular dynamics simulations; Drug-membrane interaction
Categories
Funding
- SECyT-UNC
- FONCYT-MINCyT-Argentina [1392-2017]
- MINCyT-Cordoba
- CONICET-Argentina [11220130100075CO]
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Fipronil is a widely used commercial insecticide whose action mechanism consists in blocking the influx of chloride ions through the gamma-aminobutyric acid type A receptor (GABA(A)-R), an integral membrane protein. The present study investigates the interaction of fipronil with phospholipid Langmuir monolayers, in order to characterize the effects that its partition could exert on the physical properties of these model membranes. A combined experimental and molecular dynamics (MD) simulations approach was performed. MD simulations were conducted in such a way that they resemble an experimental compression isotherm of DPPC in the presence of fipronil in the aqueous subphase. Both the experimental and the simulated compression isotherm showed that the partition of fipronil between DPPC molecules induces an expansion of the monolayer. Experimental results also showed that fipronil can penetrate lipid monolayers even in condensed packing states. MD simulations showed that fipronil induces an ordering effect in the acyl chains of DPPC in the liquid-condensed phase. In addition, the simulations indicate that fipronil orients parallel to the plane of the monolayer and that it establishes hydrogen bonds with the glycerol region of DPPC. Free energy profiles of the partition of fipronil into the monolayers, obtained by means of umbrella sampling, indicated that its penetration is thermodynamically favorable, being the interphase between the glycerol region and the acyl chains of DPPC its most favorable location. Our results suggest that fipronil could modulate the supramolecular organization of biological membranes surrounding GABA(A)-R, contributing, at least in part, to its action mechanism.
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