Fluorescence lifetime imaging by time-correlated single-photon counting

被引:416
作者
Becker, W
Bergmann, A
Hink, MA
König, K
Benndorf, K
Biskup, C
机构
[1] Becker & Hickl GmbH, D-12277 Berlin, Germany
[2] Univ Wageningen & Res Ctr, Micro Spect Ctr, NL-6703 Wageningen, Netherlands
[3] Fraunhofer Inst Biomed Tech, D-66386 St Ingbert, Germany
[4] Univ Jena, Inst Physiol, D-07740 Jena, Germany
关键词
fluorescence lifetime imaging; FLIM; time-correlated single photon counting; TCSPC; multiphoton microscopy; confocal microscopy; multi-wavelength; fluorescence resonance energy transfer; FRET;
D O I
10.1002/jemt.10421
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We present a time-correlated single photon counting (TCPSC) technique that allows time-resolved multi-wavelength imaging in conjunction with a laser scanning microscope and a pulsed excitation source. The technique is based on a four-dimensional histogramming process that records the photon density over the time of the fluorescence decay, the x-y coordinates of the scanning area, and the wavelength. The histogramming process avoids any time gating or wavelength scanning and, therefore, yields a near-perfect counting efficiency. The time resolution is limited only by the transit time spread of the detector. The technique can be used with almost any confocal or two-photon laser scanning microscope and works at any scanning rate. We demonstrate the application to samples stained with several dyes and to CFP-YFP FRET.
引用
收藏
页码:58 / 66
页数:9
相关论文
共 62 条
[1]   Application Of Multiphoton steady state and lifetime imaging to mapping of tumour vascular architecture in vivo [J].
Ameer-Beg, SM ;
Barber, PR ;
Hodgkiss, RJ ;
Locke, RJ ;
Newman, RG ;
Tozer, GM ;
Vojnovic, B ;
Wilson, J .
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES II, 2002, 4620 :85-95
[2]   Fluorescence resonance energy transfer determinations using multiphoton fluorescence lifetime imaging microscopy to characterize amyloid-beta plaques [J].
Bacskai, BJ ;
Skoch, J ;
Hickey, GA ;
Allen, R ;
Hyman, BT .
JOURNAL OF BIOMEDICAL OPTICS, 2003, 8 (03) :368-375
[3]  
Baeyens WRG, 1991, LUMINESCENCE TECHNIQ
[4]   AN ERROR ANALYSIS OF THE RAPID LIFETIME DETERMINATION METHOD FOR THE EVALUATION OF SINGLE EXPONENTIAL DECAYS [J].
BALLEW, RM ;
DEMAS, JN .
ANALYTICAL CHEMISTRY, 1989, 61 (01) :30-33
[5]   FRET measurements by TCSPC laser scanning microscopy [J].
Becker, W ;
Benndorf, K ;
Bergmann, A ;
Biskup, C ;
König, K ;
Tirplapur, U ;
Zimmer, T .
PHOTON MIGRATION, OPTICAL COHERENCE TOMOGRAPHY, AND MICROSCOPY, 2001, 4431 :94-98
[6]   High count rate multichannel TCSPC for optical tomography [J].
Becker, W ;
Bergmann, A ;
Wabnitz, H ;
Grosenick, D ;
Liebert, A .
PHOTON MIGRATION, OPTICAL COHERENCE TOMOGRAPHY, AND MICROSCOPY, 2001, 4431 :249-254
[7]   Picosecond fluorescence lifetime microscopy by TCSPC imaging [J].
Becker, W ;
Bergmann, A ;
König, K ;
Tirlapur, U .
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES, 2001, 4262 :414-419
[8]   Lifetime imaging with the Zeiss LSM-510 [J].
Becker, W ;
Bergmann, A ;
Weiss, G .
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES II, 2002, 4620 :30-35
[9]   Multi-wavelength TCSPC lifetime imaging [J].
Becker, W ;
Bergmann, A ;
Biskup, C ;
Zimmer, T ;
Klöcker, N ;
Benndorf, K .
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES II, 2002, 4620 :79-84
[10]  
Berezovska O, 2003, J NEUROSCI, V23, P4560