Hink Mark A
Section of Molecular Cytology, van Leeuwenhoek Centre for Advanced Microscopy (LCAM), Swammerdam Institute for Life Sciences (SILS), University of Amsterdam, Sciencepark 904, 1098 XH, Amsterdam, The Netherlands,
Protoplasma. 2014 Mar;251(2):307-16. doi: 10.1007/s00709-013-0602-z. Epub 2014 Jan 14.
Originally developed for the field of physical chemistry, fluorescence fluctuation spectroscopy (FFS) has evolved to a family of methods to quantify concentrations, diffusion rates and interactions of fluorescently labelled molecules. The possibility to measure at the nanomolar concentration level and to combine these techniques with microscopy allow to study biological processes with high sensitivity in the living cell. In this review, the basic principles, challenges and recent developments of the most common FFS methods are being discussed and illustrated by intracellular applications.
荧光涨落光谱法(FFS)最初是为物理化学领域开发的,现已发展成为一系列用于量化荧光标记分子的浓度、扩散速率和相互作用的方法。能够在纳摩尔浓度水平进行测量,并将这些技术与显微镜相结合,使得在活细胞中以高灵敏度研究生物过程成为可能。在这篇综述中,将讨论最常见的FFS方法的基本原理、挑战和最新进展,并通过细胞内应用进行说明。