High frame rate fluorescence lifetime imaging

被引:73
作者
Agronskaia, AV
Tertoolen, L
Gerritsen, HC
机构
[1] Univ Utrecht, Debye Inst, Dept Mol Biophys, NL-3508 TA Utrecht, Netherlands
[2] Netherlands Inst Dev Biol, KNAW Hubrecht Lab, NL-3584 CT Utrecht, Netherlands
关键词
D O I
10.1088/0022-3727/36/14/301
中图分类号
O59 [应用物理学];
学科分类号
摘要
A fast time-domain based fluorescence lifetime imaging, (FLIM) microscope is presented that can operate at frame rates of hundreds of frames per second. A beam splitter in the detection path of a wide-field fluorescence microscope divides the fluorescence in two parts. One part is optically delayed with respect to the other. Both parts are viewed with a single time-gated intensified CCD camera with a gate width of 5 ns. The fluorescence lifetime image is obtained from the ratio of these two images. The fluorescence lifetime resolution of the FLIM microscope is verified both with dye solutions and fluorescent latex beads. The fluorescence lifetimes obtained from the reference specimens are in good agreement with values obtained from time correlated single photon counting measurements on the same specimens. The acquisition speed of the FLIM system is evaluated with a measurement of the calcium fluxes in neonatal rat myocytes stained with the calcium probe Oregon Green 488-Bapta. Fluorescence lifetime images of the calcium fluxes related to the beating of the myocytes are acquired with frame rates of up to 100 Hz.
引用
收藏
页码:1655 / 1662
页数:8
相关论文
共 39 条
[1]   CA2+ TRANSIENTS IN CARDIAC MYOCYTES MEASURED WITH HIGH AND LOW-AFFINITY CA2+ INDICATORS [J].
BERLIN, JR ;
KONISHI, M .
BIOPHYSICAL JOURNAL, 1993, 65 (04) :1632-1647
[2]   INTRINSIC CYTOSOLIC CALCIUM BUFFERING PROPERTIES OF SINGLE-RAT CARDIAC MYOCYTES [J].
BERLIN, JR ;
BASSANI, JWM ;
BERS, DM .
BIOPHYSICAL JOURNAL, 1994, 67 (04) :1775-1787
[3]   FLUORESCENCE LIFETIME IMAGING USING A CONFOCAL LASER SCANNING MICROSCOPE [J].
BUURMAN, EP ;
SANDERS, R ;
DRAAIJER, A ;
GERRITSEN, HC ;
VANVEEN, JJF ;
HOUPT, PM ;
LEVINE, YK .
SCANNING, 1992, 14 (03) :155-159
[4]   SPATIAL NONUNIFORMITIES IN [CA2+](I) DURING EXCITATION-CONTRACTION COUPLING IN CARDIAC MYOCYTES [J].
CANNELL, MB ;
CHENG, H ;
LEDERER, WJ .
BIOPHYSICAL JOURNAL, 1994, 67 (05) :1942-1956
[5]   SYNTHESIS AND PROPERTIES OF A POTENTIAL EXTRACELLULAR FLUORESCENT-PROBE FOR POTASSIUM [J].
CROSSLEY, R ;
GOOLAMALI, Z ;
SAMMES, PG .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1994, (07) :1615-1623
[6]   Multiple time-gate module for fluorescence lifetime imaging [J].
de Grauw, CJ ;
Gerritsen, HC .
APPLIED SPECTROSCOPY, 2001, 55 (06) :670-678
[7]   Imaging properties in two-photon excitation microscopy and effects of refractive-index mismatch in thick specimens [J].
de Grauw, GJ ;
Vroom, JM ;
van der Voort, HTM ;
Gerritsen, HC .
APPLIED OPTICS, 1999, 38 (28) :5995-6003
[8]   Fluorescence lifetime imaging with picosecond resolution for biomedical applications [J].
Dowling, K ;
Dayel, MJ ;
Lever, MJ ;
French, PMW ;
Hares, JD ;
Dymoke-Bradshaw, AKL .
OPTICS LETTERS, 1998, 23 (10) :810-812
[9]   Fluorescence imaging in the millisecond time range of membrane electropermeabilisation of single cells using a rapid ultra-low-light intensifying detection system [J].
Gabriel, B ;
Teissié, J .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1998, 27 (03) :291-298
[10]   Fluorescence lifetime imaging in scanning microscopes: acquisition speed, photon economy and lifetime resolution [J].
Gerritsen, HC ;
Asselbergs, MAH ;
Agronskaia, AV ;
Van Sark, WGJHM .
JOURNAL OF MICROSCOPY-OXFORD, 2002, 206 :218-224