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Time-Resolved Fluorescence in Lipid Bilayers: Selected Applications and Advantages over Steady State

  1. 1.
    SYSNO ASEP0436040
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTime-Resolved Fluorescence in Lipid Bilayers: Selected Applications and Advantages over Steady State
    Author(s) Amaro, Mariana (UFCH-W) RID, ORCID
    Šachl, Radek (UFCH-W) RID, ORCID
    Jurkiewicz, Piotr (UFCH-W) RID, ORCID
    Coutinho, A. (PT)
    Prieto, M. (PT)
    Hof, Martin (UFCH-W) RID, ORCID
    Source TitleBiophysical Journal. - : Cell Press - ISSN 0006-3495
    Roč. 107, č. 12 (2014), s. 2751-2760
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    Keywordsnanoparticles ; reactivity ; energetics
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGC14-03141J GA ČR - Czech Science Foundation (CSF)
    LH13259 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000346434200007
    EID SCOPUS84920127267
    DOI10.1016/j.bpj.2014.10.058
    AnnotationFluorescence methods are versatile tools for obtaining dynamic and topological information about biomembranes because the molecular interactions taking place in lipid membranes frequently occur on the same timescale as fluorescence emission. The fluorescence intensity decay, in particular, is a powerful reporter of the molecular environment of a fluorophore. The fluorescence lifetime can be sensitive to the local polarity, hydration, viscosity, and/or presence of fluorescence quenchers/ energy acceptors within several nanometers of the vicinity of a fluorophore. Illustrative examples of how time-resolved fluorescence measurements can provide more valuable and detailed information about a system than the time-integrated (steady-state) approach will be presented in this review: 1), determination of membrane polarity and mobility using time-dependent spectral shifts; 2), identification of submicroscopic domains by fluorescence lifetime imaging microscopy; 3), elucidation of membrane leakage mechanisms from dye self-quenching assays; and 4), evaluation of nanodomain sizes by time-resolved Fo¨ rster resonance energy transfer measurements.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2015
Number of the records: 1  

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