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dc.contributor.authorBrilkov, Maxim
dc.contributor.authorStenbakk, Victoria
dc.contributor.authorJakubec, Martin
dc.contributor.authorVasskog, Terje
dc.contributor.authorKristoffersen, Tone
dc.contributor.authorCavanagh, Jorunn Pauline
dc.contributor.authorEricson, Johanna Ulrica
dc.contributor.authorIsaksson, Johan Mattias
dc.contributor.authorFlaten, Gøril Eide
dc.date.accessioned2024-01-10T13:38:28Z
dc.date.available2024-01-10T13:38:28Z
dc.date.issued2023-12-13
dc.description.abstractOne way to mitigate the ongoing antimicrobial resistance crisis is to discover and develop new classes of antibiotics. As all antibiotics at some point need to either cross or just interact with the bacterial membrane, there is a need for representative models of bacterial membranes and efficient methods to characterize the interactions with novel molecules -both to generate new knowledge and to screen compound libraries. Since the bacterial cell envelope is a complex assembly of lipids, lipopolysaccharides, membrane proteins and other components, constructing relevant synthetic liposome-based models of the membrane is both difficult and expensive. We here propose to let the bacteria do the hard work for us. Bacterial extracellular vesicles (bEVs) are naturally secreted by Gram-negative and Gram-positive bacteria, playing a role in communication between bacteria, as virulence factors, molecular transport or being a part of the antimicrobial resistance mechanism. bEVs consist of the bacterial outer membrane and thus inherit many components and properties of the native outer cell envelope. In this work, we have isolated and characterized bEVs from one Escherichia coli mutant and three clinical strains of the ESKAPE pathogens Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa. The bEVs were shown to be representative models for the bacterial membrane in terms of lipid composition with speciesstrain specific variations. The bEVs were further used to probe the interactions between bEV and antimicrobial peptides (AMPs) as model compounds by Surface Plasmon Resonance (SPR) and provide proof-of-principle that bEVs can be used as an easily accessible and highly realistic model for the bacterial surface in interaction studies. This further enables direct monitoring of the effect induced by antibiotics, or the response to host-pathogen interactions.en_US
dc.identifier.citationBrilkov M, Stenbakk, Jakubec M, Vasskog TV, Kristoffersen T, Cavanagh JP, Ericson jue, Isaksson J, Flaten gef. Bacterial extracellular vesicles: towards realistic models for bacterial membranes in molecular interaction studies by surface plasmon resonance. Frontiers in Molecular Biosciences. 2023en_US
dc.identifier.cristinIDFRIDAID 2222034
dc.identifier.doi10.3389/fmolb.2023.1277963
dc.identifier.issn2296-889X
dc.identifier.urihttps://hdl.handle.net/10037/32404
dc.language.isoengen_US
dc.publisherFrontiers Mediaen_US
dc.relation.journalFrontiers in Molecular Biosciences
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleBacterial extracellular vesicles: towards realistic models for bacterial membranes in molecular interaction studies by surface plasmon resonanceen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)