Optimizing imaging parameters for the separation of multiple labels in a fluorescence image

被引:97
作者
Neher, R [1 ]
Neher, E [1 ]
机构
[1] Max Planck Inst Biophys Chem, D-37070 Gottingen, Germany
来源
JOURNAL OF MICROSCOPY-OXFORD | 2004年 / 213卷
关键词
emission fingerprinting; fluorescence lifetime imaging (FLIM); fluorescence resonance energy transfer (FRET); fluorescent protein; laser scan microscopy; photobleaching; separation of fluorophores; spectral unmixing;
D O I
10.1111/j.1365-2818.2004.01262.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
A theoretical analysis is presented on how to separate the contributions from individual, simultaneously present fluorophores in a spectrally resolved image. Equations are derived that allow the calculation of the signal-to-noise ratio of the estimates for such contributions, given the spectral information on the individual fluorophores, the excitation wavelengths and intensities, and the number and widths of the spectral detection channels. We then ask how such imaging parameters have to be chosen for optimal fluorophore separation. We optimize the signal-to-noise ratio or optimize a newly defined 'figure of merit', which is a measure of efficiency in the use of emitted photons. The influence of photobleaching on the resolution and on the choice of imaging parameters is discussed, as well as the additional resolution gained by including fluorescence lifetime information. A surprisingly small number of spectral channels are required for an almost optimal resolution, if the borders of these channels are optimally selected. The detailed consideration of photobleaching is found to be essential, whenever there is significant bleaching. Consideration of fluorescence lifetime information (in addition to spectral information) improves results, particularly when lifetimes differ by more than a factor of two.
引用
收藏
页码:46 / 62
页数:17
相关论文
共 19 条
[1]  
BODEWIG E, 1959, MATRIX CALCULUS
[2]  
CLEGG RM, 1992, P SOC PHOTO-OPT INS, V1640, P448, DOI 10.1117/12.58237
[3]   Preassociation of calmodulin with voltage-gated Ca2+ channels revealed by FRET in single living cells [J].
Erickson, MG ;
Alseikhan, BA ;
Peterson, BZ ;
Yue, DT .
NEURON, 2001, 31 (06) :973-985
[4]   *ZWISCHENMOLEKULARE ENERGIEWANDERUNG UND FLUORESZENZ [J].
FORSTER, T .
ANNALEN DER PHYSIK, 1948, 2 (1-2) :55-75
[5]  
Garini Y, 1999, CYTOMETRY, V35, P214, DOI 10.1002/(SICI)1097-0320(19990301)35:3<214::AID-CYTO4>3.0.CO
[6]  
2-D
[7]   Autofluorescent proteins in single-molecule research: Applications to live cell imaging microscopy [J].
Harms, GS ;
Cognet, L ;
Lommerse, PHM ;
Blab, GA ;
Schmidt, T .
BIOPHYSICAL JOURNAL, 2001, 80 (05) :2396-2408
[8]   Multispectral imaging fluorescence microscopy for living cells [J].
Hiraoka, Y ;
Shimi, T ;
Haraguchi, T .
CELL STRUCTURE AND FUNCTION, 2002, 27 (05) :367-374
[9]  
KESHAVA N, 2000, IEEE SIG P MAG JAN, P44
[10]   Resolution of multiple green fluorescent protein color variants and dyes using two-photon microscopy and imaging spectroscopy [J].
Lansford, R ;
Bearman, G ;
Fraser, SE .
JOURNAL OF BIOMEDICAL OPTICS, 2001, 6 (03) :311-318