首页> 外文会议>Conference on Multiphoton Microscopy in the Biomedical Sciences III Jan 26-28, 2003 San Jose, California, USA >Thermal bleaching in single fluorescent molecules under two-photon excitation regime
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Thermal bleaching in single fluorescent molecules under two-photon excitation regime

机译:双光子激发下单个荧光分子的热漂白

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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:单分子光谱法通常需要将分子固定在固体或准固体基质上,并使用相对较高的激发强度。我们已经研究了用于生物成像研究的四种常见染料,若丹明6g,荧光素,pyr和indo-1在双光子激发条件下在单分子水平的荧光发射。我们专注于对单个分子的稳定性的双光子激发热效应,影响内部光动力学和荧光发射的总持续时间。通过旋涂在玻璃基板上扩散的单个染料分子显示出恒定的荧光输出,直到突然过渡到黑暗状态为止。 g的时间从最快的到最慢的依次在in,印度1,荧光素和若丹明6g系列中变化,并且具有高斯分布,表明漂白不是由于光漂白引起的。这些观察结果被解释为热漂白,其中通过双光子激发过程引起温度升高,并且该热漂白与未被重新辐射为荧光的吸收功率的量相关。

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