Characterization of probe binding and comparison of its influence on fluorescence lifetime of two pH-sensitive benzo[c]xanthene dyes using intensity-modulated multiple-wavelength scanning technique

被引:19
作者
Andersson, RM [1 ]
Carlsson, K
Liljeborg, A
Brismar, H
机构
[1] Karolinska Inst, Astrid Lindgren Childrens Hosp, Res Lab Q2 09, Dept Woman & Child Hlth, SE-17176 Stockholm, Sweden
[2] Royal Inst Technol, Dept Biomed & Xray Phys, SE-10044 Stockholm, Sweden
[3] Royal Inst Technol, Dept Phys & Nanostruct, SE-10044 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
confocal microscopy; fluorescence lifetime imaging; pH measurement; COS-7; SNAFL-1; SNAFL-2;
D O I
10.1006/abio.2000.4652
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantitative pH imaging using the carboxy semi-naphthofluorescein dyes SNAFL-1 and SNAFL-2 can be performed by measurement of intensity ratios or fluorescence lifetimes. However, there is a controversy as to whether the latter method has the practical advantage of a straightforward pH calibration in buffers compared to a cumbersome and time-consuming procedure in cells. In this study we have undertaken a systematic study of the potential factors influencing the fluorescence lifetime of the probes at different pH using confocal microscopy. In vitro results demonstrate that factors such as lipid and protein concentrations have a substantial influence on pH measurements based on fluorescence lifetime. The pH could be overestimated by more than 2 pH units. Studies in permeabilized COS-7 cells demonstrate the same trends as observed in the in vitro studies. (C) 2000 Academic Press.
引用
收藏
页码:104 / 110
页数:7
相关论文
共 17 条
[1]   Fluorescence lifetime imaging of pH in cells: investigation of factors influencing the pH calibration lifetime [J].
Andersson, RM ;
Carlsson, K ;
Liljeborg, A ;
Brismar, H .
OPTICAL DIAGNOSTICS OF LIVING CELLS III, 2000, 3921 :242-248
[2]  
Andersson RM, 1998, ACTA PHYSIOL SCAND, V164, P39
[3]   CONFOCAL SCANNING MICROFLUOROMETRY OF DUAL-LABELED SPECIMENS USING 2 EXCITATION WAVELENGTHS AND LOCK-IN DETECTION TECHNIQUE [J].
ASLUND, N ;
CARLSSON, K .
MICRON, 1993, 24 (06) :603-609
[4]  
Carlsson K, 1998, J MICROSC-OXFORD, V191, P119, DOI 10.1046/j.1365-2818.1998.00362.x
[5]   Signal-to-noise ratio for confocal microscopy when the intensity-modulated multiple-beam scanning (IMS) technique [J].
Carlsson, K .
MICRON, 1995, 26 (04) :317-322
[6]   Confocal fluorescence microscopy using spectral and lifetime information to simultaneously record four fluorophores with high channel separation [J].
Carlsson, K ;
Liljeborg, A .
JOURNAL OF MICROSCOPY, 1997, 185 :37-46
[7]   Method for intracellular imaging of ion concentrations, using confocal microscopy and fluorophore lifetimes [J].
Carlsson, K ;
Liljeborg, A ;
Andersson, RM ;
Brismar, H .
THREE-DIMENSIONAL AND MULTIDIMENSIONAL MICROSCOPY: IMAGE ACQUISITION PROCESSING VII, 2000, 3919 :30-37
[8]  
Krishnamoorthy G, 1997, CURR SCI INDIA, V72, P835
[9]   CYTOPLASMIC CA2+ AND H+ CONCENTRATIONS DETERMINE CELL FATE IN DICTYOSTELIUM-DISCOIDEUM [J].
KUBOHARA, Y ;
OKAMOTO, K .
FASEB JOURNAL, 1994, 8 (11) :869-874
[10]  
LILJEBORG A, 1998, P SOC PHOTO-OPT INS, V3568, P82