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Time-Resolved Fluorescence in Lipid Bilayers: Selected Applications and Advantages over Steady State
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SYSNO ASEP 0436040 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Time-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, ORCIDSource Title Biophysical Journal. - : Cell Press - ISSN 0006-3495
Roč. 107, č. 12 (2014), s. 2751-2760Number of pages 10 s. Language eng - English Country US - United States Keywords nanoparticles ; reactivity ; energetics Subject RIV CF - Physical ; Theoretical Chemistry R&D Projects GC14-03141J GA ČR - Czech Science Foundation (CSF) LH13259 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Institutional support UFCH-W - RVO:61388955 UT WOS 000346434200007 EID SCOPUS 84920127267 DOI 10.1016/j.bpj.2014.10.058 Annotation Fluorescence 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. Workplace J. Heyrovsky Institute of Physical Chemistry Contact Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Year of Publishing 2015
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