Biodynamic Optical Imaging Center (BIOPIC), Peking University , Beijing 100871, China.
School of Life Sciences, Peking University , Beijing 100871, China.
J Phys Chem B. 2017 Dec 21;121(50):11262-11272. doi: 10.1021/acs.jpcb.7b09229. Epub 2017 Dec 8.
Fluorescence correlation spectroscopy (FCS) encodes the information on the equilibrium constant (K), the relative fluorescence brightness of fluorophore (Q), and the forward and backward reaction rate constants (k and k) on a physical or chemical relaxation. However, it has been a long-standing problem to completely resolve the FCS data to get the thermodynamic and kinetic information. Recently, we have solved the problem for fluorescence autocorrelation spectroscopy (FACS). Here, we extend the method to fluorescence cross-correlation spectroscopy (FCCS), which appears when FCS is coupled with fluorescence resonance energy transfer (FRET). Among 12 total second-order and third-order pre-exponential factors in a relaxation process probed by the FRET-FCS technique, 3 are independent. We presented and discussed 3 sets of explicit solutions to use these pre-exponential factors to calculate K and Q. Together with the relaxation time, the acquired K will allow people to obtain k and k, so that the goal of deciphering the FRET-FCS data will be fully reached. The theory is verified by extensive computer simulations and tested experimentally on a system of oligonucleotide hybridization.
荧光相关光谱(FCS)将物理或化学弛豫过程中的平衡常数(K)、荧光团的相对荧光亮度(Q)以及正向和反向反应速率常数(k 和 k)的信息编码。然而,完全解析 FCS 数据以获取热力学和动力学信息一直是一个长期存在的问题。最近,我们已经解决了荧光自相关光谱(FACS)的问题。在这里,我们将该方法扩展到荧光互相关光谱(FCCS),当 FCS 与荧光共振能量转移(FRET)结合时会出现 FCCS。在 FRET-FCS 技术探测的弛豫过程中的 12 个总二阶和三阶前指数因子中,有 3 个是独立的。我们提出并讨论了 3 组明确的解,以使用这些前指数因子来计算 K 和 Q。与弛豫时间一起,获得的 K 将允许人们获得 k 和 k,从而全面实现解析 FRET-FCS 数据的目标。该理论通过广泛的计算机模拟进行了验证,并在寡核苷酸杂交系统上进行了实验测试。