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
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