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PXD041359

PXD041359 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleConformational restriction shapes the inhibition of a multidrug efflux adaptor protein
DescriptionMembrane efflux pumps play a major role in bacterial multidrug resistance. The tripartite multidrug efflux pump system from Escherichia coli, AcrAB-TolC, is a target for inhibition to lessen resistance development and restore antibiotic efficacy, with homologs in other ESKAPE pathogens. Here, we rationalize a mechanism of inhibition against the periplasmic adaptor protein, AcrA, using a combination of hydrogen/deuterium exchange mass spectrometry, cellular efflux assays, and molecular dynamics simulations. We define the structural dynamics of AcrA and find that an inhibitor can inflict long-range stabilisation across all four of its domains, whereas an interacting efflux substrate has minimal effect. Our results support a model where an inhibitor forms a molecular wedge within a cleft between the lipoyl and αβ domains of AcrA, diminishing its conformational transmission of drug-evoked signals from AcrB to TolC. This work provides molecular insights into multidrug adaptor protein function which could be valuable for developing antimicrobial therapeutics.
HostingRepositoryPRIDE
AnnounceDate2023-06-01
AnnouncementXMLSubmission_2023-06-01_07:07:46.142.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterBenjaminRussell Lewis
SpeciesList scientific name: Escherichia coli; NCBI TaxID: 562;
ModificationListNo PTMs are included in the dataset
InstrumentQ Exactive HF; SYNAPT G2-Si; Xevo G2-XS QTof
Dataset History
RevisionDatetimeStatusChangeLog Entry
02023-04-05 15:12:47ID requested
12023-06-01 07:07:46announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: Membrane proteins,Multidrug efflux pump, Efflux pump inhibitors, HDX-MS
Contact List
EamonnReading
contact affiliationDepartment of Chemisty, Redaing Group, King's College London
contact emaileamonn.reading@kcl.ac.uk
lab head
BenjaminRussell Lewis
contact affiliationKing's College London
contact emailbenjamin.russell_lewis@kcl.ac.uk
dataset submitter
Full Dataset Link List
Dataset FTP location
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