Quantitative imaging of protein-protein interactions by multiphoton fluorescence lifetime imaging microscopy using a streak camera

被引:63
作者
Krishnan, RV [1 ]
Masuda, A [1 ]
Centonze, VE [1 ]
Herman, B [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Struct & Cellular Biol, San Antonio, TX 78229 USA
关键词
fluorescence lifetime imaging microscopy;
D O I
10.1117/1.1577574
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence lifetime imaging microscopy (FLIM) using multiphoton excitation techniques is now finding an important place in quantitative imaging of protein-protein interactions and intracellular physiology. Recent developments in multiphoton FLIM methods are reviewed and a novel multiphoton FLIM system using a streak camera is described. An example of a typical application of the system is provided in which the fluorescence resonance energy transfer between a donor-acceptor pair of fluorescent proteins within a cellular specimen is measured. (C) 2003 Society of Photo-Optical Instrumentation Engineers.
引用
收藏
页码:362 / 367
页数:6
相关论文
共 34 条
[1]   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
[2]   Dynamic fluorescence anisotropy imaging microscopy in the frequency domain (rFLIM) [J].
Clayton, AHA ;
Hanley, QS ;
Arndt-Jovin, DJ ;
Subramaniam, V ;
Jovin, TM .
BIOPHYSICAL JOURNAL, 2002, 83 (03) :1631-1649
[3]  
Clegg Robert M., 1995, Current Opinion in Biotechnology, V6, P103, DOI 10.1016/0958-1669(95)80016-6
[4]   Time-domain whole-field fluorescence lifetime imaging with optical sectioning [J].
Cole, MJ ;
Siegel, J ;
Webb, SED ;
Jones, R ;
Dowling, K ;
Dayel, MJ ;
Parsons-Karavassilis, D ;
French, PMW ;
Lever, MJ ;
Sucharov, LOD ;
Neil, MAA ;
Juskaitis, R ;
Wilson, T .
JOURNAL OF MICROSCOPY, 2001, 203 (03) :246-257
[5]   Nanosecond fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy to localize the protein interactions in a single living cell [J].
Elangovan, M ;
Day, RN ;
Periasamy, A .
JOURNAL OF MICROSCOPY, 2002, 205 :3-14
[6]   Two-photon fluorescence lifetime imaging microscopy of macrophage-mediated antigen processing [J].
French, T ;
So, PTC ;
Weaver, DJ ;
CoelhoSampaio, T ;
Gratton, E ;
Voss, EW ;
Carrero, J .
JOURNAL OF MICROSCOPY-OXFORD, 1997, 185 :339-353
[7]   OLIGOMERIZATION OF EPIDERMAL GROWTH-FACTOR RECEPTORS ON A431 CELLS STUDIED BY TIME-RESOLVED FLUORESCENCE IMAGING MICROSCOPY - A STEREOCHEMICAL MODEL FOR TYROSINE KINASE RECEPTOR ACTIVATION [J].
GADELLA, TWJ ;
JOVIN, TM .
JOURNAL OF CELL BIOLOGY, 1995, 129 (06) :1543-1558
[8]   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
[9]   Imaging FRET between spectrally similar GFP molecules in single cells [J].
Harpur, AG ;
Wouters, FS ;
Bastiaens, PIH .
NATURE BIOTECHNOLOGY, 2001, 19 (02) :167-169
[10]   Development of wide-field, multi-imaging x-ray streak camera technique with increased image-sampling arrays [J].
Heya, M ;
Fujioka, S ;
Shiraga, H ;
Miyanaga, N ;
Yamanaka, T .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2001, 72 (01) :755-758