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Intramolecular Triplet Quenching by Nitroxide Radicals as a Tool for Determining Peptide Secondary Structure in Solution

机译:硝基氧化物基团的分子内三态细胞作为用于测定溶液中肽二级结构的工具

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Quenching of the excited states of a chromophore by a suitable moiety can provide important information on the probe-quencher distance. Singlet quenching through Forster energy transfer has been exploited by us in the determination of the structural features of many ordered oligopeptides in solution, by combining experimental data with molecular modeling studies. Quenching of excited triplet states would extend this approach from the nanoseconds time-region of singlet lifetimes to the microseconds, possibly providing new insights on peptide dynamics. To verify the scope of this method, we have investigated the distance dependence of the intramolecular quenching of the benzophenone triplet of the Bpa residue by the nitroxide radical of TO AC in the oligopeptides listed in Figure 1.
机译:通过合适的部分淬火发色细胞的激发态可以提供关于探针猝灭距离的重要信息。 通过组合具有分子建模研究的实验数据,我们通过福尔斯特能量转移通过福尔斯特能量转移来利用福尔斯特能量转移来确定溶液中许多有序寡肽的结构特征。 激发的三重态状态的淬火将从单次寿命的纳秒的时间区域扩展到微秒,可能为肽动力学提供新的见解。 为了验证该方法的范围,我们研究了在图1中列出的寡肽中的硝基氧化物基团的二氧化物基团的二苯甲酮三体的分子内猝灭的距离依赖性。

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