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Thioamide Quenching of Fluorescent Probes Through Photoinduced Electron Transfer: Mechanistic Studies and Applications

机译:通过光诱导电子转移的荧光探针的硫酰胺淬灭:机理研究和应用。

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摘要

Previously we have shown that thioamides can be incorporated into proteins as minimally perturbing fluorescence- quenching probes to study protein dynamics, folding, and aggregation. Here, we show that the spontaneity of photoinduced electron transfer between a thioamide and an excited fluorophore is governed by the redox potentials of each moiety according to a Rehm-Weller-type model. We have used this model to predict thioamide quenching of various common fluorophores, and we rigorously tested more than a dozen examples. In each case, we found excellent agreement between our theoretical predictions and experimental observations. In this way, we have been able to expand the scope of fluorophores quenched by thioamides to include dyes suitable for microscopy and single molecule studies, including fluorescein, Alexa Fluor 488, BODIPY FL, and rhodamine 6G. We describe the photochemistry of these systems and explore applications that demonstrate the utility of thioamide quenching of fluorescein to studying protein folding and proteolysis.
机译:先前我们已经证明,硫酰胺可以作为干扰最小的荧光猝灭探针掺入蛋白质中,以研究蛋白质的动力学,折叠和聚集。在这里,我们表明,根据Rehm-Weller型模型,硫酰胺和激发的荧光团之间的光诱导电子转移的自发性受每个部分的氧化还原电势支配。我们已经使用该模型预测了各种常见荧光团的硫酰胺猝灭,并严格测试了十多个示例。在每种情况下,我们都在理论预测和实验观察之间找到了极好的一致性。通过这种方式,我们已经能够扩大被硫酰胺淬灭的荧光团的范围,使其包括适用于显微镜和单分子研究的染料,包括荧光素,Alexa Fluor 488,BODIPY FL和若丹明6G。我们描述了这些系统的光化学,并探索了证明荧光素的硫代酰胺猝灭作用用于研究蛋白质折叠和蛋白水解作用的应用。

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