Waitt Advanced Biophotonics Center, Salk Institute for Biological Studies, La Jolla, CA 92037, United States.
Curr Opin Struct Biol. 2011 Oct;21(5):650-60. doi: 10.1016/j.sbi.2011.06.006. Epub 2011 Jul 21.
Fluorescence correlation spectroscopy (FCS) is a minimally invasive real-time fluorescence technique capable of detecting single molecules in vitro and in situ. By recording and correlating the fluctuations in fluorescence intensity measurements, it is possible to obtain information on molecular mobility and diffusion, hydrodynamic radii, local concentrations and photochemical and photophysical properties. By using dual-color cross-correlation spectroscopy, it is possible to monitor highly specific molecular-level interactions such as binding processes and chemical reactions. Recent advances in alternative detection schemes have allowed the extension of these techniques to the monitoring of slower timescales (e.g. Raster Image Correlation Spectroscopy-RICS) or higher concentrations (e.g. Total Internal Reflection-TIR-FCS). Given the versatility of these techniques, they have become commonplace tools used to specifically unravel the spatio-temporal dynamics of macromolecular entities in living biological systems.
荧光相关光谱学(FCS)是一种微创实时荧光技术,能够在体外和原位检测单分子。通过记录和相关荧光强度测量的波动,有可能获得关于分子流动性和扩散、水动力半径、局部浓度以及光化学和光物理性质的信息。通过使用双色互相关光谱学,可以监测高度特异性的分子水平相互作用,如结合过程和化学反应。替代检测方案的最新进展允许将这些技术扩展到监测较慢的时间尺度(例如,光栅图像相关光谱学-RICS)或更高的浓度(例如,全内反射-TIR-FCS)。鉴于这些技术的多功能性,它们已成为常用工具,用于专门揭示活生物系统中大分子实体的时空动态。