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Molecular interpretation of fluorescence solvent relaxation of Patman and 2H NMR experiments in phosphatidylcholine bilayers

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    SYSNO ASEP0084818
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleMolecular interpretation of fluorescence solvent relaxation of Patman and 2H NMR experiments in phosphatidylcholine bilayers
    TitleInterpretace relaxace rozpouštědla Patmanu a 2H NMR eperimentů ve fosfatidylcholinových membránách na molekulární úrovni
    Author(s) Olžyńska, Agnieszka (UFCH-W) RID
    Zań, Anna (UFCH-W)
    Jurkiewicz, Piotr (UFCH-W) RID, ORCID
    Sýkora, Jan (UFCH-W) RID
    Gröbner, G. (SE)
    Langner, M. (PL)
    Hof, Martin (UFCH-W) RID, ORCID
    Source TitleChemistry and Physics of Lipids. - : Elsevier - ISSN 0009-3084
    Roč. 147, č. 2 (2007), s. 69-77
    Number of pages9 s.
    Languageeng - English
    CountryIE - Ireland
    Keywordssolvent relaxation ; 2H NMR ; Patman ; lipid hydration ; unsaturated hydrocarbon chain
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsIAA400400503 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GA203/05/2308 GA ČR - Czech Science Foundation (CSF)
    GD203/05/H001 GA ČR - Czech Science Foundation (CSF)
    LC06063 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Next sourceOther public resources
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    DOI10.1016/j.chemphyslip.2007.03.004
    AnnotationThe analysis of time-dependent fluorescence shifts of the bilayer probe 6-hexadecanoyl-2-(((2-(trimethylammonium)ethyl)methyl)amino)naphthalene chloride (Patman) offers valuable information on the hydration and dynamics of phospholipid headgroups. Quenching studies on vesicles composed of four phosphatidylcholines with different hydrocarbon chains (18:1c9/18:1c9, DOPC; 16:0/18:1c9, POPC; 18:1c9/16:0, OPPC; 18:1c6/18:1c6, PC.DELTA.6) show that the chromophore of Patman is defined located at the level of the sn-1 ester-group in the phospholipid, which is invariant to the hydrocarbon chain. The so-called solvent relaxation (SR) approach as well as solid-state 2H NMR reveals that DOPC and PCΔ6 are more hydrated than POPC and OPPC. A strong dependence of SR kinetics on the position of double bond in the investigated fatty acid chains was observed. Apparently, the closer the double bond is located to the hydrated sn-1 ester-group, the more mobile this group becomes.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2008
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