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Single-Molecule Spectroscopy inside an Optical Cavity

机译:光腔内部的单分子光谱

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摘要

Dynamic structural changes of macromolecules undergoing biochemical reactions can be studied using a novel single pair fluorescence resonance energy transfer (sp-FRET) tool which can be used as a nanoscale spectroscopic ruler. Although recent advances in applying such a nanoscale ruler to biological systems have been made, improvements in photon detectors and photophysical properties of the single FRET pair are still being studied. Motivated by the recent progresses in single-atom laser, we have investigated the ability to use the optical microcavity to amplify the sp-FRET signal. When the single FRET pair and the attached macromolecule of interest are placed inside an optical cavity with the emission mode of the acceptor dye in resonance with the cavity mode, quantitative modeling shows that, when adjusting the acceptor-cavity coupling parameters to be appropriate values, the acceptor fluorescence emission signal amplified by the cavity coupling mode would reach a significant value, leading to a much brighter sp-FRET spectroscopic signal. Possible applications to sp-FRET measurement of biological molecules are quantitatively examined.
机译:可以使用新颖的单对荧光共振能量转移(sp-FRET)工具研究可以进行大分子动态化学结构变化的生化反应,该工具可以用作纳米级光谱尺。尽管已经取得了将这种纳米级标尺应用于生物系统的最新进展,但仍在研究单FRET对的光子检测器和光物理性质的改进。受单原子激光器最新进展的推动,我们研究了使用光学微腔来放大sp-FRET信号的能力。当将单个FRET对和连接的感兴趣的大分子置于光腔内时,受体染料的发射模式与腔模式共振,定量建模表明,将受体-腔耦合参数调整为适当值时,通过腔耦合模式放大的受体荧光发射信号将达到显着值,从而导致更亮的sp-FRET光谱信号。定量检查了sp-FRET测量生物分子的可能应用。

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