Practical guidelines for dual-color fluorescence cross-correlation spectroscopy

被引:194
作者
Bacia, Kirsten [1 ]
Schwille, Petra [1 ]
机构
[1] Tech Univ Dresden, Dept Biophys, BIOTEC, D-01307 Dresden, Germany
关键词
D O I
10.1038/nprot.2007.410
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dual-color fluorescence cross-correlation spectroscopy (FCCS) allows for the determination of molecular mobility and concentrations and for the quantitative analysis of molecular interactions such as binding or cleavage at very low concentrations. This protocol discusses considerations for preparing a biological system for FCCS experiments and offers practical advice for performing FCCS on a commercially available setup. Although FCCS is closely related to two-color confocal microscopy, critical adjustments and test measurements are necessary to establish successful FCCS measurements, which are described in a step-by-step manner. Moreover, we discuss control experiments for a negative cross-correlation artifact, arising from a lack of detection volume overlap, and a positive artifact, arising from cross-talk. FCCS has been applied to follow molecular interactions in solutions, on membranes and in cells and to analyze dynamic colocalization during intracellular transport. It is a technique that is expected to see new applications in various fields of biochemical and cell biological research.
引用
收藏
页码:2842 / 2856
页数:15
相关论文
共 54 条
[1]   Fluorescence cross-correlation spectroscopy in living cells [J].
Bacia, K ;
Kim, SA ;
Schwille, P .
NATURE METHODS, 2006, 3 (02) :83-89
[2]   A dynamic view of cellular processes by in vivo fluorescence auto- and cross-correlation spectroscopy [J].
Bacia, K ;
Schwille, P .
METHODS, 2003, 29 (01) :74-85
[3]   SNAREs prefer liquid-disordered over "raft" (liquid-ordered) domains when reconstituted into giant unilamellar vesicles [J].
Bacia, K ;
Schuette, CG ;
Kahya, N ;
Jahn, R ;
Schwille, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (36) :37951-37955
[4]   Probing the endocytic pathway in live cells using dual-color fluorescence cross-correlation analysis [J].
Bacia, K ;
Majoul, IV ;
Schwille, P .
BIOPHYSICAL JOURNAL, 2002, 83 (02) :1184-1193
[5]  
BACIA K, 2007, LIPID RAFTS, pCH7
[6]   Two-hybrid fluorescence cross-correlation spectroscopy detects protein-protein interactions in vivo [J].
Baudendistel, N ;
Müller, G ;
Waldeck, W ;
Angel, P ;
Langowski, J .
CHEMPHYSCHEM, 2005, 6 (05) :984-990
[7]   C-terminal fluorescence labeling of proteins for interaction studies on the single-molecule level [J].
Becker, Christian F. W. ;
Seidel, Ralf ;
Jahnz, Michael ;
Bacia, Kirsten ;
Niederhausen, Thomas ;
Alexandrov, Kirill ;
Schwille, Petra ;
Goody, Roger S. ;
Engelhard, Martin .
CHEMBIOCHEM, 2006, 7 (06) :891-895
[8]   The photon counting histogram in fluorescence fluctuation spectroscopy [J].
Chen, Y ;
Müller, JD ;
So, PTC ;
Gratton, E .
BIOPHYSICAL JOURNAL, 1999, 77 (01) :553-567
[9]   Diffusion coefficient measurements in microfluidic devices [J].
Culbertson, CT ;
Jacobson, SC ;
Ramsey, JM .
TALANTA, 2002, 56 (02) :365-373
[10]  
Davis Lloyd M., 2003, Current Pharmaceutical Biotechnology, V4, P451, DOI 10.2174/1389201033377337