Department of Physics and Biological Physics Research Group, University of Oxford, Parks Road, Oxford OX1 3PU, UK.
Chemphyschem. 2010 Jul 12;11(10):2209-19. doi: 10.1002/cphc.201000129.
Probability distribution analysis (PDA) is a recently developed statistical tool for predicting the shapes of single-molecule fluorescence resonance energy transfer (smFRET) histograms, which allows the identification of single or multiple static molecular species within a single histogram. We used a generalized PDA method to predict the shapes of FRET histograms for molecules interconverting dynamically between multiple states. This method is tested on a series of model systems, including both static DNA fragments and dynamic DNA hairpins. By fitting the shape of this expected distribution to experimental data, the timescale of hairpin conformational fluctuations can be recovered, in good agreement with earlier published results obtained using different techniques. This method is also applied to studying the conformational fluctuations in the unliganded Klenow fragment (KF) of Escherichia coli DNA polymerase I, which allows both confirmation of the consistency of a simple, two-state kinetic model with the observed smFRET distribution of unliganded KF and extraction of a millisecond fluctuation timescale, in good agreement with rates reported elsewhere. We expect this method to be useful in extracting rates from processes exhibiting dynamic FRET, and in hypothesis-testing models of conformational dynamics against experimental data.
概率分布分析(PDA)是一种最近开发的统计工具,用于预测单分子荧光共振能量转移(smFRET)直方图的形状,它可以在单个直方图中识别单个或多个静态分子种类。我们使用广义 PDA 方法来预测在多个状态之间动态相互转化的分子的 FRET 直方图的形状。该方法在一系列模型系统上进行了测试,包括静态 DNA 片段和动态 DNA 发夹。通过将预期分布的形状拟合到实验数据中,可以恢复发夹构象波动的时间尺度,与使用不同技术获得的早期发表结果非常吻合。该方法还应用于研究未结合的大肠杆菌 DNA 聚合酶 I 的 Klenow 片段(KF)的构象波动,这不仅证实了简单的两态动力学模型与未结合 KF 的观察到的 smFRET 分布的一致性,而且还提取了毫秒波动时间尺度,与其他地方报道的速率非常吻合。我们期望该方法可用于从表现出动态 FRET 的过程中提取速率,并根据实验数据对构象动力学模型进行假设检验。