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Molecular interpretation of fluorescence solvent relaxation of Patman and 2H NMR experiments in phosphatidylcholine bilayers
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SYSNO ASEP 0084818 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Ostatní články Title Molecular interpretation of fluorescence solvent relaxation of Patman and 2H NMR experiments in phosphatidylcholine bilayers Title Interpretace 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, ORCIDSource Title Chemistry and Physics of Lipids. - : Elsevier - ISSN 0009-3084
Roč. 147, č. 2 (2007), s. 69-77Number of pages 9 s. Language eng - English Country IE - Ireland Keywords solvent relaxation ; 2H NMR ; Patman ; lipid hydration ; unsaturated hydrocarbon chain Subject RIV CF - Physical ; Theoretical Chemistry R&D Projects IAA400400503 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 source Other public resources CEZ AV0Z40400503 - UFCH-W (2005-2011) DOI 10.1016/j.chemphyslip.2007.03.004 Annotation The 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. Workplace J. Heyrovsky Institute of Physical Chemistry Contact Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Year of Publishing 2008
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