Four-dimensional multiphoton microscopy with time-correlated single-photon counting

被引:45
作者
Schönle, A [1 ]
Glatz, M [1 ]
Hell, SW [1 ]
机构
[1] Max Planck Inst Biophys Chem, High Resolut Opt Microscopy Grp, D-37070 Gottingen, Germany
关键词
D O I
10.1364/AO.39.006306
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We report on the implementation of fluorescence-lifetime imaging in multiphoton excitation microscopy that uses PC-compatible modules for time-correlated single-photon counting. Four-dimensional data stacks are produced with each pixel featuring fluorescence-decay curves that consist of as many as 4096 bins. Fluorescence lifetime(s) and their amplitude(s) are extracted by statistical methods at each pixel or in arbitrarily defined regions of interest. When employing an avalanche photodiode the width of the temporal response function is 420 ps. Although this response confines the temporal resolution to values greater than several hundreds of picoseconds, the lifetime precision is determined by the signal-to-noise ratio and can be in the range of tens of picosconds. Lifetime changes are visualized in pulsed-laser-deposited fluorescent layers as well as in cyan fluorescent proteins that transfer energy to yellow fluorescent proteins in live mammalian cells. (C) 2000 Optical Society of America. OCIS codes: 110.0110, 120.4640, 170.6320, 180.2520.
引用
收藏
页码:6306 / 6311
页数:6
相关论文
共 17 条
[1]   Imaging the intracellular trafficking and state of the AB(5) quaternary structure of cholera toxin [J].
Bastiaens, PIH ;
Majoul, IV ;
Verveer, PJ ;
Soling, HD ;
Jovin, TM .
EMBO JOURNAL, 1996, 15 (16) :4246-4253
[2]   Time-resolved detection and identification of single analyte molecules in microcapillaries by time-correlated single-photon counting (TCSPC) [J].
Becker, W ;
Hickl, H ;
Zander, C ;
Drexhage, KH ;
Sauer, M ;
Siebert, S ;
Wolfrum, J .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1999, 70 (03) :1835-1841
[3]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[4]  
Draaijer A., 1995, P491
[5]   Ultrafast dynamics microscopy [J].
Dyba, M ;
Klar, TA ;
Jakobs, S ;
Hell, SW .
APPLIED PHYSICS LETTERS, 2000, 77 (04) :597-599
[6]   PULSED-LASER FLUOROPHORE DEPOSITION - A METHOD FOR MEASURING THE AXIAL RESOLUTION IN 2-PHOTON FLUORESCENCE MICROSCOPY [J].
HELL, SW ;
UTZ, AR ;
SCHRADER, M ;
HANNINEN, PE ;
SOINI, E .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 1995, 12 (09) :2072-2076
[7]   LIFETIME-SELECTIVE FLUORESCENCE IMAGING USING AN RF PHASE-SENSITIVE CAMERA [J].
LAKOWICZ, JR ;
BERNDT, KW .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1991, 62 (07) :1727-1734
[8]   FLUORESCENCE LIFETIME IMAGING OF FREE AND PROTEIN-BOUND NADH [J].
LAKOWICZ, JR ;
SZMACINSKI, H ;
NOWACZYK, K ;
JOHNSON, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (04) :1271-1275
[9]   TIME RESOLVED IMAGING MICROSCOPY - PHOSPHORESCENCE AND DELAYED FLUORESCENCE IMAGING [J].
MARRIOTT, G ;
CLEGG, RM ;
ARNDTJOVIN, DJ ;
JOVIN, TM .
BIOPHYSICAL JOURNAL, 1991, 60 (06) :1374-1387
[10]  
MORGAN CG, 1991, J MICROSC, V165, P49