Laurdan and Di-4-ANEPPDHQ probe different properties of the membrane

被引:113
作者
Amaro, Mariana [1 ]
Reina, Francesco [2 ]
Hof, Martin [1 ]
Eggeling, Christian [2 ]
Sezgin, Erdinc [2 ]
机构
[1] CAS, J Heyrovsky Inst Phys Chem, Vvi, Dept Biophys Chem, Dolejskova 3, Prague 18223, Czech Republic
[2] Univ Oxford, MRC Human Immunol Unit, Oxford OX3 9DS, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
cell membrane; lipid packing; laurdan; di-4-ANEPPDHQ; time-dependent fluorescence shift; liposomes; GPMVs; PHOSPHOLIPID-BILAYERS; SOLVENT RELAXATION; SOLVATION DYNAMICS; LIPID PACKING; CELL-MEMBRANES; LIVING CELLS; CHOLESTEROL; FLUORESCENCE; VESICLES; FLUIDITY;
D O I
10.1088/1361-6463/aa5dbc
中图分类号
O59 [应用物理学];
学科分类号
摘要
Lipid packing is a crucial feature of cellular membranes. Quantitative analysis of membrane lipid packing can be achieved using polarity sensitive probes whose emission spectrum depends on the lipid packing. However, detailed insights into the exact mechanisms that cause the changes in the spectra are necessary to interpret experimental fluorescence emission data correctly. Here, we analysed frequently used polarity sensitive probes, Laurdan and di-4-ANEPPDHQ, to test whether the underlying physical mechanisms of their spectral changes are the same and, thus, whether they report on the same physico-chemical properties of the cell membrane. Steady-state spectra as well as time-resolved emission spectra of the probes in solvents and model membranes revealed that they probe different properties of the lipid membrane. Our findings are important for the application of these dyes in cell biology.
引用
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页数:9
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