Short-lived fluorescence component of DPH reports on lipid--water interface of biological membranes
Jazyk angličtina Země Irsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15172830
DOI
10.1016/j.chemphyslip.2004.02.005
PII: S0009308404000271
Knihovny.cz E-zdroje
- MeSH
- 1,2-dipalmitoylfosfatidylcholin farmakologie MeSH
- benzylalkohol farmakologie MeSH
- časové faktory MeSH
- difenylhexatrien analýza chemie MeSH
- ethanol farmakologie MeSH
- fluorescence MeSH
- fluorescenční polarizace MeSH
- lipidy chemie MeSH
- liposomy chemie MeSH
- teplota MeSH
- voda chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1,2-dipalmitoylfosfatidylcholin MeSH
- benzylalkohol MeSH
- difenylhexatrien MeSH
- ethanol MeSH
- lipidy MeSH
- liposomy MeSH
- voda MeSH
Fluorescence measurements of 1,6-diphenyl-1,3,5-hexatriene (DPH) in large unilamellar phospholipid vesicles were performed to characterize the influence of the membrane physical properties on the short-lived lifetime component of the fluorescence decay. We have found that the short-lived component of DPH significantly shortens when the membrane undergoes a temperature-induced phase transition as it is known for the long-lived component of DPH. We induced membrane phase transitions also by alcohols, which are reported to be distributed different way in the membrane--ethanol close to the membrane-water interface and benzyl alcohol in the membrane core. A different effect of the respective alcohol on the short and long decay component was observed. Both the time-resolved fluorescence spectra of DPH taken during lipid vesicle staining and the lifetime dependences caused by changes of temperature and/or induced by the alcohols show that the short-lived fluorescence originates from the population of dye molecules distributed at the membrane-water interface.
Citace poskytuje Crossref.org