Imaging molecular interactions in living cells by FRET microscopy

被引:244
作者
Jares-Erijman, Elizabeth A.
Jovin, Thomas M.
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Organ, Ciudad Univ, RA-1428 Buenos Aires, DF, Argentina
[2] Max Planck Inst Biophys Chem, Dept Mol Biol, D-37077 Gottingen, Germany
关键词
D O I
10.1016/j.cbpa.2006.08.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forster resonance energy transfer (FRET) is applied extensively in all fields of biological research and technology, generally as a 'nanoruler' with a dynamic range corresponding to the intramolecular and intermolecular distances characterizing the molecular structures that regulate cellular function. The complex underlying network of interactions reflects elementary reactions operating under strict spatio-temporal control: binding, conformational transition, covalent modification and transport. FRET imaging provides information about all these molecular processes with high specificity and sensitivity via probes expressed by or introduced from the external medium into the cell, tissue or organism. Current approaches and developments in the field are discussed with emphasis on formalism, probes and technical implementation.
引用
收藏
页码:409 / 416
页数:8
相关论文
共 98 条
[11]   Energy dissipation in multichromophoric single dendrimers [J].
De Schryver, FC ;
Vosch, T ;
Cotlet, M ;
Van der Auweraer, M ;
Müllen, K ;
Hofkens, J .
ACCOUNTS OF CHEMICAL RESEARCH, 2005, 38 (07) :514-522
[12]  
Dumas D, 2005, CLIN HEMORHEOL MICRO, V33, P293
[13]   Multi-dimensional time-correlated single photon counting (TCSPC) fluorescence lifetime imaging microscopy (FLIM) to detect FRET in cells [J].
Duncan, RR ;
Bergmann, A ;
Cousin, MA ;
Apps, DK ;
Shipston, MJ .
JOURNAL OF MICROSCOPY, 2004, 215 :1-12
[14]   Analysis of photobleaching in single-molecule multicolor excitation and forster resonance energy transfer measurement [J].
Eggeling, C ;
Widengren, J ;
Brand, L ;
Schaffer, J ;
Felekyan, S ;
Seidel, CAM .
JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (09) :2979-2995
[15]   Performance of fluorescence correlation spectroscopy for measuring diffusion and concentration [J].
Enderlein, J ;
Gregor, I ;
Patra, D ;
Dertinger, T ;
Kaupp, UB .
CHEMPHYSCHEM, 2005, 6 (11) :2324-2336
[16]   Fluorescence lifetime heterogeneity resolution in the frequency domain by lifetime moments analysis [J].
Esposito, A ;
Gerritsen, HC ;
Wouters, FS .
BIOPHYSICAL JOURNAL, 2005, 89 (06) :4286-4299
[17]  
ESPOSITO A, 2004, CURR PROTOCOLS CELL
[18]   Innovating lifetime microscopy: a compact and simple tool for life sciences, screening, and diagnostics [J].
Esposito, Alessandro ;
Gerritsen, Hans C. ;
Oggier, Thierry ;
Lustenberger, Felix ;
Wouters, Fred S. .
JOURNAL OF BIOMEDICAL OPTICS, 2006, 11 (03)
[19]   Biosensors based on binding-modulated donor-acceptor distances [J].
Fan, CH ;
Plaxco, KW ;
Heeger, AJ .
TRENDS IN BIOTECHNOLOGY, 2005, 23 (04) :186-192
[20]   A dark yellow fluorescent protein (YFP)-based Resonance Energy-Accepting Chromoprotein (REACh) for Forster resonance energy transfer with GFP [J].
Ganesan, S ;
Ameer-beg, SM ;
Ng, TTC ;
Vojnovic, B ;
Wouters, FS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (11) :4089-4094