Abstract

Oecophylla smaragdina, a biological pest control agent attacks its prey with their mandibles followed by ejection of venom; rendering them paralyzed. Even though Oecophylla smaragdina is a successful pest control agent, no attempts have been made to outline its molecular mechanism of action hitherto. The first part of this study intends characterization of venom constituents using preliminary methods followed by coupled gas chromatography and mass spectroscopy (GC–MS) analysis. The results indicate the anticipated presence of neurotoxin in ant venom (2,5-dipropyl-decahydroquinoline). This alkaloid is a known non-competitive inhibitor of nicotinic acetylcholine receptors (nAChRs), but the proper mechanism of inhibition by decahydroquinoline was obscure and has been addressed in this study. Based on the results and known facts, the second part of this study deals with in silico docking and molecular dynamics simulations to portray the molecular level inhibition of nAChRs by decahydroquinolines. Molecular docking and dynamics studies indicate that the inhibition of nAChRs by decahydroquinoline is attained by occluding the pore lumen of nAChRs in the serine–leucine ring. The GC–MS analysis followed by in silico studies thereby indicates that the potent non-competitive inhibitor of nAChRs found in the venom of Oecophylla must be posing paralyzing effects on its prey.

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