Fluorescence resonance energy transfer imaging microscopy.

作者: Victoria E. Centonze , Mao Sun , Atsushi Masuda , Hans Gerritsen , Brian Herman

DOI: 10.1016/S0076-6879(03)60127-8

关键词:

摘要: Publisher Summary This chapter describes the fluorescence resonance energy transfer (FRET) imaging microscopy. RET is a process by which donor fluorophore (D) in its excited state may excitation to nearby chromophore (acceptor, A). The nonradiative (not mediated photon) and achieved through dipole–dipole interactions. In principle, for such occur, several major criteria must be satisfied. First, molecule have an emission spectrum that overlaps absorption of acceptor molecule. second criterion needs satisfied molecules within 10–100 A each other. efficiency between falls off as sixth power distance separating molecules. Another met lifetime sufficient duration allow FRET occur. Continued research this area needed determine optimal approaches measurement development more refined algorithms analysis data.

参考文章(36)
Brian Herman, X. F. Wang, Fluorescence imaging spectroscopy and microscopy J. Wiley. ,(1996)
Sarah Rice, Abel W. Lin, Daniel Safer, Cynthia L. Hart, Nariman Naber, Bridget O. Carragher, Shane M. Cain, Elena Pechatnikova, Elizabeth M. Wilson-Kubalek, Michael Whittaker, Edward Pate, Roger Cooke, Edwin W. Taylor, Ronald A. Milligan, Ronald D. Vale, A structural change in the kinesin motor protein that drives motility Nature. ,vol. 402, pp. 778- 784 ,(1999) , 10.1038/45483
Albert Cha, Gregory E. Snyder, Paul R. Selvin, Francisco Bezanilla, Atomic scale movement of the voltage-sensing region in a potassium channel measured via spectroscopy Nature. ,vol. 402, pp. 809- 813 ,(1999) , 10.1038/45552
Ailsa G. Harpur, Fred S. Wouters, Philippe I.H. Bastiaens, Imaging FRET between spectrally similar GFP molecules in single cells Nature Biotechnology. ,vol. 19, pp. 167- 169 ,(2001) , 10.1038/84443
P. I. Bastiaens, I. V. Majoul, P. J. Verveer, H. D. Söling, T. M. Jovin, Imaging the intracellular trafficking and state of the AB5 quaternary structure of cholera toxin. The EMBO Journal. ,vol. 15, pp. 4246- 4253 ,(1996) , 10.1002/J.1460-2075.1996.TB00799.X
Rosario Rizzuto, Marisa Brini, Paola Pizzo, Marta Murgia, Tullio Pozzan, Chimeric green fluorescent protein as a tool for visualizing subcellular organelles in living cells Current Biology. ,vol. 5, pp. 635- 642 ,(1995) , 10.1016/S0960-9822(95)00128-X
Peter J. Verveer, Anthony Squire, Philippe I.H. Bastiaens, Global analysis of fluorescence lifetime imaging microscopy data. Biophysical Journal. ,vol. 78, pp. 2127- 2137 ,(2000) , 10.1016/S0006-3495(00)76759-2
Yi-Kang Hu, Jack H. Kaplan, Site-directed Chemical Labeling of Extracellular Loops in a Membrane Protein Journal of Biological Chemistry. ,vol. 275, pp. 19185- 19191 ,(2000) , 10.1074/JBC.M000641200
Xue Feng Wang, Ammasi Periasamy, Brian Herman, David M. Coleman, Fluorescence Lifetime Imaging Microscopy (FLIM): Instrumentation and Applications Critical Reviews in Analytical Chemistry. ,vol. 23, pp. 369- 395 ,(1992) , 10.1080/10408349208051651