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Counting tagged molecules one by one: Quantitative photoactivation and bleaching of photoactivatable fluorophores

机译:一对一标记分子的数量:光活化荧光团的定量光活化和漂白

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摘要

Determining the number of molecules in a given assembly, such as the number of proteins in a toxic aggregate, is often critical to understanding chemistry and function. Herein, we report a variation of a limitless method for counting photoactivatable fluorescent dyes in which single dye molecules are photoswitched to a fluorescent state, counted, and then irreversibly photobleached. We use this method to count the number of CAGE 552 covalently bound to the surface of 500 nm polystyrene beads. Activation of CAGE 552 was achieved with a 405 nm laser pulse. Once activated, the dye was excited with 532 nm light, and the fluorescence emission was collected with a CCD camera. The results from the fluorescence experiments were then compared to bulk fluorescence measurements to assess the error in counting. There are other ways of counting molecules, such as photobleaching and statistical analysis of reversible switchable chromophores. The method reported here provides a lower bound to the number of chromophores, with no upper limit to the number of molecules that can be quantified.
机译:确定给定装配体中的分子数量(例如有毒聚集体中的蛋白质数量)通常对于理解化学和功能至关重要。本文中,我们报告了一种用于计数可光活化荧光染料的无限方法的变化形式,其中将单个染料分子光转换为荧光状态,进行计数,然后不可逆地进行光漂白。我们使用这种方法计算与500 nm聚苯乙烯珠粒表面共价结合的CAGE 552的数量。用405 nm激光脉冲激活了CAGE 552。活化后,染料用532 nm光激发,并用CCD相机收集荧光发射。然后将荧光实验的结果与体荧光测量结果进行比较,以评估计数误差。还有其他计数分子的方法,例如光漂白和可逆可转换生色团的统计分析。此处报道的方法对发色团的数量提供了下限,而对可量化分子的数量没有上限。

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