Anthony Neil, Berland Keith
Department of Physics, Emory University, Atlanta, Georgia, USA.
Methods Enzymol. 2013;518:145-73. doi: 10.1016/B978-0-12-388422-0.00007-8.
Fluorescence correlation spectroscopy (FCS) and related fluctuation spectroscopy and microscopy methods have become important research tools that enable detailed investigations of the chemical and physical properties of molecules and molecular systems in a variety of complex environments. Information recovery via curve fitting of fluctuation data can present complicating challenges due to limited resolution and/or problems with fitting model verification. We discuss a new approach to data analysis called τFCS that couples multiple modes of signal acquisition, here specifically FCS and fluorescence lifetimes, with global analysis. We demonstrate enhanced resolution using τFCS, including the capability to recover the concentration of both molecular species in a two-component mixture even when the species have identical diffusion coefficients and molecular brightness values, provided their fluorescent lifetimes are distinct. We also demonstrate how τFCS provides useful tools for model discrimination in FCS curve fitting.
荧光相关光谱法(FCS)以及相关的波动光谱法和显微镜方法已成为重要的研究工具,能够在各种复杂环境中对分子和分子系统的化学和物理性质进行详细研究。由于分辨率有限和/或拟合模型验证存在问题,通过波动数据曲线拟合进行信息恢复可能会带来复杂的挑战。我们讨论了一种名为τFCS的数据分析新方法,该方法将多种信号采集模式(在此具体为FCS和荧光寿命)与全局分析相结合。我们展示了使用τFCS提高的分辨率,包括即使两种组分具有相同的扩散系数和分子亮度值,但只要它们的荧光寿命不同,就能恢复两组分混合物中两种分子物种浓度的能力。我们还展示了τFCS如何为FCS曲线拟合中的模型判别提供有用工具。