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End-to-End Diffusion and Distance Distributions of Flexible Donor–Acceptor Systems Observed by Intramolecular Energy Transfer and Frequency-Domain Fluorometry; Enhanced Resolution by Global Analysis of Externally Quenched and Nonquenched Samples

机译:分子内能量转移和频域荧光法观察柔性供体-受体系统的端到端扩散和距离分布;通过对外部淬火和非淬火的样品进行全局分析来提高分辨率

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摘要

We used time-dependent fluorescence energy transfer of externally quenched and nonquenched samples, and global analysis of the data, to recover the end-to-end distance distributions and diffusion coefficients of flexible fluorescent molecules in low-viscosity solution. The fluorescence decays of tryptamine covalently linked to a dansyl acceptor by a polyethylene chain of 22 methylene groups were measured by the frequency-domain method. The data were fitted using numerical solutions of the diffusion equation which predicts the time- and distance-dependent population of the excited-state donors in the presence of energy transfer, followed by transformation to the frequency domain for nonlinear least-squares fitting to the experimental data. From the simulation study we found that the time- and distance-dependent population of the excited-state donors are significantly different for nonquenched and quenched samples and that the effects of end-to-end diffusion on the donor decay is decreased by collisional quenching. Importantly, the resolution is dramatically improved by the use of simultaneous analysis of quenched and nonquenched samples. This method was applied to the tryptamine–dansyl system using acrylamide as an external quencher. The recovered initial (t = 0) distance distribution, Rav = 18.9 Å, hw = 17.1 Å, is very similar to that obtained for diffusion-free conditions. The end-to-end diffusion coefficient of D = 1.26 × 10−5 cm2/s is comparable to that expected for molecules the size of indole and dansyl. This value is about twice smaller than that obtained from diffusion-dependent intermolecular energy transfer using unlinked indole and dansylamide as the donor and acceptor, respectively, which may reflect the effects of the linker on diffusion of the chromophores.
机译:我们使用外部淬灭和非猝灭样品的时间依赖性荧光能量转移以及数据的整体分析,以恢复低粘度溶液中柔性荧光分子的端到端距离分布和扩散系数。通过频域法测量通过22个亚甲基的聚乙烯链共价连接至丹磺酰基受体的色胺的荧光衰减。使用扩散方程的数值解拟合数据,该方程可预测在存在能量转移的情况下受激态供体的时间和距离相关的总体,然后转换为频域以对实验进行非线性最小二乘拟合数据。从模拟研究中我们发现,对于非猝灭和淬灭的样品,激发态供体的时间和距离相关种群显着不同,并且碰撞猝灭降低了端对端扩散对供体衰变的影响。重要的是,通过同时分析淬灭和非淬灭的样品,可显着提高分离度。该方法用于使用丙烯酰胺作为外部淬灭剂的色胺-丹磺酰基体系。恢复的初始(t = 0)距离分布Rav = 18.9Å,hw = 17.1Å,与在无扩散条件下获得的非常相似。 D的端到端扩散系数= 1.26×10 -5 cm 2 / s与吲哚和丹磺酰基大小的分子的预期相近。该值比使用未连接的吲哚和丹磺酰胺分别作为供体和受体的依赖于扩散的分子间能量转移所获得的值小大约两倍,这可能反映了接头对发色团扩散的影响。

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