Fluctuations as a source of information in fluorescence microscopy

被引:17
作者
Petrasek, Zdenek [1 ]
Schwille, Petra [1 ]
机构
[1] Tech Univ Dresden, Biophys Grp, Biotechnol Zentrum, D-01307 Dresden, Germany
关键词
fluorescence spectroscopy; imaging; single molecule; IMAGE CORRELATION SPECTROSCOPY; SINGLE-MOLECULE FLUORESCENCE; CROSS-CORRELATION SPECTROSCOPY; RESONANCE ENERGY-TRANSFER; INTENSITY DISTRIBUTION ANALYSIS; PHOTON ARRIVAL TRAJECTORIES; LASER-SCANNING MICROSCOPE; PARTICLE TRACKING; LIVING CELLS; HIGH-ORDER;
D O I
10.1098/rsif.2008.0200.focus
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluctuations in fluorescence spectroscopy and microscopy have traditionally been regarded as noise they lower the resolution and contrast and do not permit high acquisition rates. However, fluctuations can also be used to gain additional information about a system. This fact has been exploited in single-point microscopic techniques, such as fluorescence correlation spectroscopy and analysis of single molecule trajectories, and also in the imaging field, e. g. in spatio-temporal image correlation spectroscopy. Here, we discuss how fluctuations are used to obtain more quantitative information from the data than that given by average values, while minimizing the effects of noise due to stochastic photon detection.
引用
收藏
页码:S15 / S25
页数:11
相关论文
共 97 条
[1]   Direct determination of kinetic rates from single-molecule photon arrival trajectories using hidden Markov models [J].
Andrec, M ;
Levy, RM ;
Talaga, DS .
JOURNAL OF PHYSICAL CHEMISTRY A, 2003, 107 (38) :7454-7464
[2]   Separating structural heterogeneities from stochastic variations in fluorescence resonance energy transfer distributions via photon distribution analysis [J].
Antonik, M ;
Felekyan, S ;
Gaiduk, A ;
Seidel, CAM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (13) :6970-6978
[3]   Fluorescence cross-correlation spectroscopy in living cells [J].
Bacia, K ;
Kim, SA ;
Schwille, P .
NATURE METHODS, 2006, 3 (02) :83-89
[4]   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
[5]   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
[6]   Fluorescence lifetime images and correlation spectra obtained by multidimensional time-correlated single photon counting [J].
Becker, W ;
Bergmann, A ;
Haustein, E ;
Petrasek, Z ;
Schwille, P ;
Biskup, C ;
Kelbauskas, L ;
Benndorf, K ;
Klöcker, N ;
Anhut, T ;
Riemann, I ;
König, K .
MICROSCOPY RESEARCH AND TECHNIQUE, 2006, 69 (03) :186-195
[7]   Performance bounds on single-particle tracking by fluorescence modulation [J].
Berglund, AJ ;
Mabuchi, H .
APPLIED PHYSICS B-LASERS AND OPTICS, 2006, 83 (01) :127-133
[8]   Tracking-FCS: Fluorescence correlation spectroscopy of individual particles [J].
Berglund, AJ ;
Mabuchi, H .
OPTICS EXPRESS, 2005, 13 (20) :8069-8082
[9]  
Berne BJ., 2000, DYNAMIC LIGHT SCATTE
[10]   Imaging intracellular fluorescent proteins at nanometer resolution [J].
Betzig, Eric ;
Patterson, George H. ;
Sougrat, Rachid ;
Lindwasser, O. Wolf ;
Olenych, Scott ;
Bonifacino, Juan S. ;
Davidson, Michael W. ;
Lippincott-Schwartz, Jennifer ;
Hess, Harald F. .
SCIENCE, 2006, 313 (5793) :1642-1645