Fluorescence fluctuation microscopy: a diversified arsenal of methods to investigate molecular dynamics inside cells

被引:19
|
作者
Weidemann, Thomas [1 ]
Muecksch, Jonas [1 ]
Schwille, Petra [1 ]
机构
[1] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
IMAGE CORRELATION SPECTROSCOPY; CROSS-CORRELATION SPECTROSCOPY; LIGAND-BINDING; LIVE CELLS; DIFFUSION; REVEALS; RECEPTOR; NUMBER; AGGREGATION; BRIGHTNESS;
D O I
10.1016/j.sbi.2014.07.008
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
Fluorescence microscopy provides insight into the subcellular organization of biological functions. However, images are snap shots averaging over a highly dynamic molecular system. Fluorescence fluctuation microscopy, employing similar detection technology, encompasses a powerful arsenal of analysis tools that investigate the molecular heterogeneity in space and time. Analyzing signal fluctuations from small ensembles (several hundred particles) reveals their concentration, the stoichiometry, the stochastic motion, as well as superimposed signatures of the environment such as spatial confinement and binding events. Thus, fluctuation analysis provides access to dynamic molecular properties that can be used to build physical models of cellular processes. In the last decade these methods experienced a remarkable diversification, which we revisit here with a particular focus on live cell applications.
引用
收藏
页码:69 / 76
页数:8
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