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Recognition of quinolone antibiotics by the multidrug efflux transporter MexB of<i>Pseudomonas aeruginosa</i>

Silvia Gervasoni, Giuliano Malloci, Andrea Bosin, Attilio V. Vargiu, Helen I. Zgurskaya, Paolo Ruggerone

2022Physical Chemistry Chemical Physics17 citationsDOIOpen Access PDF

Abstract

, 6919) reported a co-crystal structure of AcrB in a complex with levofloxacin, an antibiotic belonging to the important class of (fluoro)-quinolones. In this work, we performed a systematic ensemble docking campaign coupled to the cluster analysis and molecular-mechanics optimization of docking poses to study the interaction between 36 quinolone antibiotics and MexB. We additionally investigated surface complementarity between each molecule and the transporter and thoroughly assessed the computational protocol adopted against the known experimental data. Our study reveals different binding preferences of the investigated compounds towards the sub-sites of the large deep binding pocket of MexB, supporting the hypothesis that MexB substrates oscillate between different binding modes with similar affinity. Interestingly, small changes in the molecular structure translate into significant differences in MexB-quinolone interactions. All the predicted binding modes are available for download and visualization at the following link: https://www.dsf.unica.it/dock/mexb/quinolones.

Topics & Concepts

EffluxDocking (animal)QuinolonePseudomonas aeruginosaChemistryComputational biologyTransporterAntibioticsBiologyBiochemistryGeneGeneticsBacteriaMedicineNursingAntibiotic Resistance in BacteriaTuberculosis Research and EpidemiologyPneumocystis jirovecii pneumonia detection and treatment
Recognition of quinolone antibiotics by the multidrug efflux transporter MexB of<i>Pseudomonas aeruginosa</i> | Litcius