Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes

Fluorescence emission from merocyanine 540 (MC540) dimers was observed in dipalmitoylphosphatidylcholine (DPPC) vesicles. This unusual behavior was observed only for vesicles in the gel-phase state. No dimer fluorescence was observed either in monopalmitoylphosphatidylcholine (C16PC) micelles or in...

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Autores principales: Bernik, D., Tymczyszyn, E., Daraio, M.E., Negri, R.M.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00318655_v70_n1_p40_Bernik
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spelling todo:paper_00318655_v70_n1_p40_Bernik2023-10-03T14:41:33Z Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes Bernik, D. Tymczyszyn, E. Daraio, M.E. Negri, R.M. Fluorescence emission from merocyanine 540 (MC540) dimers was observed in dipalmitoylphosphatidylcholine (DPPC) vesicles. This unusual behavior was observed only for vesicles in the gel-phase state. No dimer fluorescence was observed either in monopalmitoylphosphatidylcholine (C16PC) micelles or in liquid-crystalline DPPC vesicles, indicating that dimer fluorescence efficiency increases in highly packed interfaces. The excitonic theory of Kasha was used to interpret the spectral features. The overall fluorescence quantum yield (φφ) decreases with decreasing lipid:probe ratio, not only because of the presence of a weakly fluorescent dimer that absorbs a high fraction of the total absorbed light but also due to quenching of monomer emission. This suggests the existence of probe domains. The dimer fluorescence quantum yields (φφD) were estimated in DPPC large unilamellar vesicles (LUV) and DPPC multilamellar vesicles. The dependence of φφ with probe concentration is compatible with values of φφD lower than 0.05. The dimerization equilibrium of MC540 in C16PC micelles and DPPC-LUV was also studied. Apparent dimerization equilibrium constants, Kdapp and dimer absorption spectrum were calculated in C16PC micelles for the first time. The dimerization equilibrium constant in DPPC-LUV was calculated and discussed in terms of the fraction of volume occupied by the lipid phase. Fil:Bernik, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Daraio, M.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Negri, R.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00318655_v70_n1_p40_Bernik
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description Fluorescence emission from merocyanine 540 (MC540) dimers was observed in dipalmitoylphosphatidylcholine (DPPC) vesicles. This unusual behavior was observed only for vesicles in the gel-phase state. No dimer fluorescence was observed either in monopalmitoylphosphatidylcholine (C16PC) micelles or in liquid-crystalline DPPC vesicles, indicating that dimer fluorescence efficiency increases in highly packed interfaces. The excitonic theory of Kasha was used to interpret the spectral features. The overall fluorescence quantum yield (φφ) decreases with decreasing lipid:probe ratio, not only because of the presence of a weakly fluorescent dimer that absorbs a high fraction of the total absorbed light but also due to quenching of monomer emission. This suggests the existence of probe domains. The dimer fluorescence quantum yields (φφD) were estimated in DPPC large unilamellar vesicles (LUV) and DPPC multilamellar vesicles. The dependence of φφ with probe concentration is compatible with values of φφD lower than 0.05. The dimerization equilibrium of MC540 in C16PC micelles and DPPC-LUV was also studied. Apparent dimerization equilibrium constants, Kdapp and dimer absorption spectrum were calculated in C16PC micelles for the first time. The dimerization equilibrium constant in DPPC-LUV was calculated and discussed in terms of the fraction of volume occupied by the lipid phase.
format JOUR
author Bernik, D.
Tymczyszyn, E.
Daraio, M.E.
Negri, R.M.
spellingShingle Bernik, D.
Tymczyszyn, E.
Daraio, M.E.
Negri, R.M.
Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes
author_facet Bernik, D.
Tymczyszyn, E.
Daraio, M.E.
Negri, R.M.
author_sort Bernik, D.
title Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes
title_short Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes
title_full Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes
title_fullStr Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes
title_full_unstemmed Fluorescent dimers of merocyanine 540 (MC540) in the gel phase of phosphatidylcholine liposomes
title_sort fluorescent dimers of merocyanine 540 (mc540) in the gel phase of phosphatidylcholine liposomes
url http://hdl.handle.net/20.500.12110/paper_00318655_v70_n1_p40_Bernik
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AT tymczyszyne fluorescentdimersofmerocyanine540mc540inthegelphaseofphosphatidylcholineliposomes
AT daraiome fluorescentdimersofmerocyanine540mc540inthegelphaseofphosphatidylcholineliposomes
AT negrirm fluorescentdimersofmerocyanine540mc540inthegelphaseofphosphatidylcholineliposomes
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