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Highly synergistic antimicrobial activity of magainin 2 and PGLa peptides is rooted in the formation of supramolecular complexes with lipids

  1. 1.
    SYSNO ASEP0531413
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHighly synergistic antimicrobial activity of magainin 2 and PGLa peptides is rooted in the formation of supramolecular complexes with lipids
    Author(s) Aisenbrey, Ch. (FR)
    Amaro, Mariana (UFCH-W) RID, ORCID
    Pospíšil, Petr (UFCH-W)
    Hof, Martin (UFCH-W) RID, ORCID
    Bechinger, B. (FR)
    Article number11652
    Source TitleScientific Reports. - : Nature Publishing Group - ISSN 2045-2322
    Roč. 10, č. 1 (2020)
    Number of pages13 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsxenopus-laevis ; membranes ; bilayers ; family ; model ; permeability ; enhancement ; mechanism ; diffusion ; topology
    Subject RIVCF - Physical ; Theoretical Chemistry
    OECD categoryPhysical chemistry
    R&D ProjectsGX19-26854X GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000550031900002
    EID SCOPUS85087930893
    DOI10.1038/s41598-020-68416-1
    AnnotationMagainin 2 and PGLa are cationic, amphipathic antimicrobial peptides which when added as equimolar mixture exhibit a pronounced synergism in both their antibacterial and pore-forming activities. Here we show for the first time that the peptides assemble into defined supramolecular structures along the membrane interface. The resulting mesophases are quantitatively described by state-of-the art fluorescence self-quenching and correlation spectroscopies. Notably, the synergistic behavior of magainin 2 and PGLa correlates with the formation of hetero-domains and an order-of-magnitude increased membrane affinity of both peptides. Enhanced membrane association of the peptide mixture is only observed in the presence of phophatidylethanolamines but not of phosphatidylcholines, lipids that dominate bacterial and eukaryotic membranes, respectively. Thereby the increased membrane-affinity of the peptide mixtures not only explains their synergistic antimicrobial activity, but at the same time provides a new concept to increase the therapeutic window of combinatorial drugs.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2021
    Electronic addresshttp://hdl.handle.net/11104/0310078
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