Perturbed structural dynamics underlie inhibition and altered efflux of the multidrug resistance pump AcrB.
Eamonn ReadingZainab AhdashChiara FaisVito RicciXuan Wang-KanElizabeth GrimseyJack StoneGiuliano MallociAndy M LauHeather FindlayAlbert KonijnenbergPaula J BoothPaolo RuggeroneAttilio Vittorio VargiuLaura J V PiddockArgyris PolitisPublished in: Nature communications (2020)
Resistance-nodulation-division efflux pumps play a key role in inherent and evolved multidrug resistance in bacteria. AcrB, a prototypical member of this protein family, extrudes a wide range of antimicrobial agents out of bacteria. Although high-resolution structures exist for AcrB, its conformational fluctuations and their putative role in function are largely unknown. Here, we determine these structural dynamics in the presence of substrates using hydrogen/deuterium exchange mass spectrometry, complemented by molecular dynamics simulations, and bacterial susceptibility studies. We show that an efflux pump inhibitor potentiates antibiotic activity by restraining drug-binding pocket dynamics, rather than preventing antibiotic binding. We also reveal that a drug-binding pocket substitution discovered within a multidrug resistant clinical isolate modifies the plasticity of the transport pathway, which could explain its altered substrate efflux. Our results provide insight into the molecular mechanism of drug export and inhibition of a major multidrug efflux pump and the directive role of its dynamics.
Keyphrases
- molecular dynamics simulations
- high resolution
- mass spectrometry
- multidrug resistant
- binding protein
- dna binding
- drug resistant
- staphylococcus aureus
- molecular docking
- emergency department
- liquid chromatography
- molecular dynamics
- acinetobacter baumannii
- single molecule
- amino acid
- gram negative
- high performance liquid chromatography
- transcription factor
- genome wide
- pseudomonas aeruginosa