Wide-field time-correlated single photon counting (TCSPC) microscopy with time resolution below the frame exposure time

被引:7
|
作者
Hirvonen, Liisa M. [1 ]
Petrasek, Zdenek [2 ]
Suhling, Klaus [1 ]
机构
[1] Kings Coll London, Dept Phys, London WC2R 2L5, England
[2] Max Planck Inst Biochem, Dept Cellular & Mol Biophys, D-82152 Martinsried, Germany
关键词
Fluorescence lifetime imaging; Single photon counting; Image intensifier; PROTEIN-PROTEIN INTERACTIONS; LIVING CELLS; LUMINESCENCE;
D O I
10.1016/j.nima.2014.09.082
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Fast frame rale CMOS cameras in combination with photon counting intensifiers can be used for fluorescence imaging with single photon sensitivity at kHz frame rates. We show here how the phosphor decay of the image intensifier can be exploited for accurate timing of photon arrival well below the camera exposure time This is achieved by taking ratios of the intensity of the photon events in two subsequent frames, and effectively allows wide-field TCSPC. This technique was used for measuring decays of ruthenium compound Ru(dpp) with lifetimes as low as 1 mu s with 18.5 mu s frame exposure time, including in living HeLa cells, using around 0.1 mu W excitation power. We speculate that by using an image intensifier with a faster phosphor decay to match a higher camera frame rate, photon arrival time measurements on the nanosecond time scale could well be possible. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
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