Elson E L
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Traffic. 2001 Nov;2(11):789-96. doi: 10.1034/j.1600-0854.2001.21107.x.
Fluorescence correlation spectroscopy (FCS) can measure dynamics of fluorescent molecules in cells. FCS measures the fluctuations in the number of fluorescent molecules in a small volume illuminated by a thin beam of excitation light. These fluctuations are processed statistically to yield an autocorrelation function from which rates of diffusion, convection, chemical reaction, and other processes can be extracted. The advantages of this approach include the ability to measure the mobility of a very small number of molecules, even down to the single molecule level, over a wide range of rates in very small regions of a cell. In addition to rates of diffusion and convection, FCS also provides unique information about the local concentration, states of aggregation and molecular interaction using fluctuation amplitude and cross-correlation methods. Recent advances in technology have rendered these once difficult measurements accessible to routine use in cell biology and biochemistry. This review provides a summary of the FCS method and describes current areas in which the FCS approach is being extended beyond its original scope.
荧光相关光谱法(FCS)可测量细胞中荧光分子的动力学。FCS测量由一束细激发光照射的小体积内荧光分子数量的波动。对这些波动进行统计处理以产生自相关函数,从中可以提取扩散、对流、化学反应及其他过程的速率。这种方法的优点包括能够在细胞的非常小的区域内,在很宽的速率范围内测量极少数分子的迁移率,甚至低至单分子水平。除了扩散和对流速率外,FCS还使用波动幅度和互相关方法提供有关局部浓度、聚集状态和分子相互作用的独特信息。技术上的最新进展使这些曾经困难的测量在细胞生物学和生物化学中得以常规使用。本综述总结了FCS方法,并描述了当前FCS方法正被扩展到其原始范围之外的领域。