Fluorescence of nitrobenzoxadiazole (NBD)-labeled lipids in model membranes is connected not to lipid mobility but to probe location

被引:51
|
作者
Amaro, Mariana [1 ]
Filipe, Hugo A. L. [2 ,3 ,4 ]
Ramalho, J. P. Prates [5 ,6 ]
Hof, Martin [1 ]
Loura, Luis M. S. [2 ,4 ,7 ]
机构
[1] Acad Sci Czech Republ, Dept Biophys Chem, J Heyrovsky Inst Phys Chem, Vvi, Dolejskova 3, CR-18223 Prague, Czech Republic
[2] Ctr Quim Coimbra, Rua Larga, P-3004535 Coimbra, Portugal
[3] Univ Coimbra, Dept Quim, Fac Ciencias & Tecnol, Rua Larga, P-3004535 Coimbra, Portugal
[4] Univ Coimbra, Ctr Neurociencias & Biol Celular, P-3004504 Coimbra, Portugal
[5] Univ Evora, Dept Quim, Escola Ciencias & Tecnol, Rua Roma Ramalho,59, P-7000671 Evora, Portugal
[6] Univ Evora, Ctr Quim Evora, Escola Ciencias & Tecnol, Rua Roma Ramalho 59, P-7000671 Evora, Portugal
[7] Univ Coimbra, Fac Farm, Polo Ciencias Saude, P-3000548 Coimbra, Portugal
关键词
MOLECULAR-DYNAMICS SIMULATIONS; TIME-RESOLVED FLUORESCENCE; DENSITY-FUNCTIONAL THEORY; N-(7-NITROBENZ-2-OXA-1,3-DIAZOL-4-YL)-LABELED LIPIDS; PHOSPHOLIPID-BILAYERS; SOLVATION DYNAMICS; PHASE-TRANSITION; EXCITED-STATES; FATTY AMINES; CHOLESTEROL;
D O I
10.1039/c5cp05238f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nitrobenzoxadiazole (NBD)-labeled lipids are popular fluorescent membrane probes. However, the understanding of important aspects of the photophysics of NBD remains incomplete, including the observed shift in the emission spectrum of NBD-lipids to longer wavelengths following excitation at the red edge of the absorption spectrum (red-edge excitation shift or REES). REES of NBD-lipids in membrane environments has been previously interpreted as reflecting restricted mobility of solvent surrounding the fluorophore. However, this requires a large change in the dipole moment (Delta mu) of NBD upon excitation. Previous calculations of the value of Delta mu of NBD in the literature have been carried out using outdated semi-empirical methods, leading to conflicting values. Using up-to-date density functional theory methods, we recalculated the value of Dm and verified that it is rather small (similar to 2 D). Fluorescence measurements confirmed that the value of REES is similar to 16 nm for 1,2-dioleoyl-sn-glycero-3-phospho-L-serine-N-(NBD) (NBD-PS) in dioleoylphosphatidylcholine vesicles. However, the observed shift is independent of both the temperature and the presence of cholesterol and is therefore insensitive to the mobility and hydration of the membrane. Moreover, red-edge excitation leads to an increased contribution of the decay component with a shorter lifetime, whereas time-resolved emission spectra of NBD-PS displayed an atypical blue shift following excitation. This excludes restrictions to solvent relaxation as the cause of the measured REES and TRES of NBD, pointing instead to the heterogeneous transverse location of probes as the origin of these effects. The latter hypothesis was confirmed by molecular dynamics simulations, from which the calculated heterogeneity of the hydration and location of NBD correlated with the measured fluorescence lifetimes/REES. Globally, our combination of theoretical and experiment-based techniques has led to a considerably improved understanding of the photophysics of NBD and a reinterpretation of its REES in particular.
引用
收藏
页码:7042 / 7054
页数:13
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