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Thermal bleaching in single fluorescent molecules under two-photon excitation regime

机译:在双光子激励制度下单荧光分子中的热漂白

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Single molecule spectroscopy often requires the immobilization of the molecules onto solid or quasi-solid substrates and the use of relatively high excitation intensity. We have studied the fluorescence emission of four common dyes used for bio-imaging studies, rhodamine 6g, fluorescein, pyrene and indo-1 at the single molecule level under two-photon excitation regime. We focus on two-photon excitation thermal effects on the stability of the single molecules, influencing the internal photo-dynamics and the total duration of the fluorescent emission. Single dye molecules, spread on a glass substrate by spin coating, show a constant fluorescence output till a sudden transition to a dark state. The bleaching time varies in the series pyrene, indo-1, fluorescein and rhodamine 6g from the fastest to the slowest one respectively, and has a gaussian distribution suggesting that bleaching is not due to photo-bleaching. These observations are interpreted as thermal bleaching where the temperature increase is induced by the two-photon excitation process and the thermal bleaching is correlated to the amount of absorbed power that is not re-irradiated as fluorescence.
机译:单分子光谱通常需要将分子固定到固体或准固体基材上并使用相对高的激发强度。我们已经研究了在双光子激励制度下的单分子水平下用于生物成像研究,罗丹明6g,荧光素,芘和Indo-1的四种常见染料的荧光发射。我们专注于对单个分子稳定性的双光子励磁热效应,影响内部光电动力学和荧光发射的总持续时间。单染料分子通过旋转涂层涂在玻璃基板上,显示出恒定的荧光输出,直至突然过渡到黑暗状态。漂白时间分别从最快到最慢的芘,印度-1,荧光素和罗达胺6g各种各样的芘,印度-1,荧光素和罗丹明6g各种各样的蛋解,并且具有高斯分布,表明漂白不是由于光漂白。这些观察结果被解释为热漂白,其中通过双光子激发过程诱导温度升高,热漂白与未被重新照射为荧光的吸收功率的量相关。

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