Abstract
AbstractBackground:The emergence of antibiotic-resistant pathogens generates impairment to human health. U1-SCTRX-lg1a is a peptide isolated from a phospholipase D extracted from the spider venom ofLoxosceles gauchowith antimicrobial activity against Gram-negative bacteria (between 1.15 μM to 4.6 μM). The aim of this study was to suggest potential receptors associated with the antimicrobial activity of U1-SCTRX-lg1a usingin silicobioinformatics tools.Methods:The search for potential targets of U1-SCRTX-lg1a was performed using the PharmMapper server. Molecular docking between U1-SCRTX-lg1a and the receptor was performed using PatchDock software. The prediction of ligand sites for each receptor was conducted using the PDBSum server. Chimera 1.6 software was used to perform molecular dynamics simulations only for the best dock score receptor. In addition, U1-SCRTX-lg1a and native ligand interactions were compared using AutoDock Vina software. Finally, predicted interactions were compared with the ligand site previously described in the literature.Results and discussion:The bioprospecting of U1-SCRTX-lg1a resulted in the identification of forty-nine intracellular proteins originating from Gram-negative microorganisms. Among these, NH3-dependent NAD+synthetase showed the highest dock score. This result suggests that the peptide derived from brown spider venom may interact with residues SER48 and THR160. In addition, the C-terminus has greater affinity for the receptor than the N-terminus.Conclusion:Thein silicobioprospecting of receptors suggests that U1-SCRTX-lg1a may interfere with NAD+production inEscherichia coli, a Gram-negative bacterium, altering the homeostasis of the microorganism and impairing growth.
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Publisher
Research Square Platform LLC
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