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dc.rights.licenseopenen_US
dc.contributor.authorLE GUERN, Florent
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorOUK, Tan-Sothea
dc.contributor.authorOUK, Catherine
dc.contributor.authorVANDERESSE, Regis
dc.contributor.authorCHAMPAVIER, Yves
dc.contributor.authorPINAULT, Emilie
dc.contributor.authorSOL, Vincent
dc.date.accessioned2021-07-16T09:54:34Z
dc.date.available2021-07-16T09:54:34Z
dc.date.issued2018
dc.identifier.issn1948-5875en_US
dc.identifier.otherhttps://pubs.acs.org/doi/abs/10.1021/acsmedchemlett.7b00360en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/109279
dc.description.abstractEnIn order to highlight the potential of photodynamic antimicrobial chemotherapy in case of infections by antibiotic resistant-strains, a new antimicrobial peptide conjugate has been synthesized, consisting of a derivative of polymyxin B and a cationic porphyrin covalently attached together to a spacer. A polymyxin-derived moiety was subjected to a primary structural modification in the replacement of four diaminobutyrate residues with lysine ones. This modification was done in order to strongly reduce bactericidal activity, with the aim to eliminate the potential rise of polymyxin-resistant strains. Despite this modification, this new conjugate displayed a strong photobactericidal activity against Gram-positive as well as Gram-negative bacteria. It was further shown that this conjugate was able to strongly stick to the cell walls of either kind of strain, thus helping to inactivate bacteria through the production of reactive oxygen species under light irradiation.
dc.language.isoENen_US
dc.subject.enPAC
dc.subject.enT cationic porphyrin
dc.subject.enpolymyxin B
dc.subject.entargeting
dc.subject.enlysine
dc.subject.enantimicrobial peptide
dc.title.enLysine Analogue of Polymyxin B as a Significant Opportunity for Photodynamic Antimicrobial Chemotherapy
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acsmedchemlett.7b00360en_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalAcs Medicinal Chemistry Lettersen_US
bordeaux.page11-16en_US
bordeaux.volume9en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN, UMR 5248)en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-02058215
hal.exportfalse
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