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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Diffusion-Photodynamics Coupling in Fluorescence Correlation Spectroscopy Studies of Photoswitchable Green Fluorescent Proteins: An Analytical and Simulative Study
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Diffusion-Photodynamics Coupling in Fluorescence Correlation Spectroscopy Studies of Photoswitchable Green Fluorescent Proteins: An Analytical and Simulative Study

机译:光开关绿色荧光蛋白的荧光相关光谱中的扩散-光动力学耦合研究:分析和模拟研究

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The photodynamics of the Green Fluorescent Protein (GFP) has been addressed in detail, particularly by means of Fluorescence Correlation Spectroscopy (FCS), a technique that provides direct information when the diffusion and the photodynamics time scales are well separated. Efficient photoswitchable GFPs, a crucial component for applications in nanoscopy imaging, have long residence times in the dark state, typically longer than the diffusion time of the protein through the observation volume. In these cases, the effect of the couplingbetween photodynamics and the diffusion process on the analysis of the FCS measurements cannot be disregarded, and the use or FCS methods becomes therefore critical. This work deals with the analytical and simulative study of such coupling and indicates that the corrections to be applied to the conventional decoupled FCS model scale as the square root of the ratio between the diffusion and the dark state relaxation times. We discuss the possibility to estimate the extent of the diffusion/photodynamics coupling from the analysis of the inverse of the fluorescence autocorrelation function g(t), defined as G~(-1) (g(t)) = g(0)/g(t) - 1. The function G~(-1)(g{t)) is analyzed in terms of a parabolic expansion in which the curvature term directly provides the desired measure of the coupling. We validate the analytical prediction and the graphical estimate of the coupling on simulations of FCS experiments that are based on a coupled Monte Carlo-Brownian Dynamics algorithm. The analysis of the curvature of G~(-1)(g(t)), applied to experimental FCS data of the photoswitchable E222Q mutant of GFPMut2 (Mut2Q), indicates that the trapping rate for this chromophore is 3 orders of magnitude underestimated when the diffusion/photodynamics coupling is not taken into account and sheds some additional light on the complex energy diagram for this protein.
机译:绿色荧光蛋白(GFP)的光动力学已经得到了详细解决,特别是通过荧光相关光谱(FCS),一种在扩散和光动力学时间尺度很好地分离时提供直接信息的技术。高效的光开关GFP是纳米显微镜成像中应用的关键组件,在黑暗状态下的停留时间较长,通常比蛋白质在观察体积中的扩散时间更长。在这些情况下,不能忽略光动力学和扩散过程之间的耦合对FCS测量分析的影响,因此使用或FCS方法变得至关重要。这项工作处理了这种耦合的分析和模拟研究,并指出了要应用于常规解耦FCS模型尺度的校正是扩散与暗态弛豫时间之比的平方根。我们讨论了通过分析荧光自相关函数g(t)的反函数来估计扩散/光动力学耦合程度的可能性,该函数定义为G〜(-1)(g(t))= g(0)/ g(t)-1.根据抛物线展开来分析函数G〜(-1)(g {t)),其中曲率项直接提供所需的耦合量度。我们在基于耦合蒙特卡洛-布朗动力学算法的FCS实验模拟中验证耦合的分析预测和图形估计。对G〜(-1)(g(t))曲率的分析应用于GFPMut2(Mut2Q)的可光转换E222Q突变体的实验FCS数据,表明该生色团的捕获率比被检测时低3个数量级。不考虑扩散/光动力学耦合,并且在该蛋白质的复杂能图中揭示了一些其他信息。

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