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Dual-Color Fluorescence Fluctuation Spectroscopy in vitro and in vivo

机译:体内外双色荧光波动光谱

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The combination of dual-color fluorescence correlation spectroscopy (FCS) and two-photon excitation is a powerful tool for probing protein-protein interactions. The submicron resolution and single molecule sensitivity of the technique make it attractive for in vivo applications. However, the strong spectral cross talk between the two emission channels of most fluorescent dye mixtures provides a challenge for the analysis of dual-color FCS experiments. We describe a new technique, dual-color photon counting histogram (PCH) analysis that overcomes some of the challenges associated with spectral cross talk. Dual-color PCH is an extension of regular PCH that simultaneously analyses the photon counts of two detection channels. We demonstrate that dual color PCH quantitatively resolves protein mixtures in vitro. We also apply dual-color PCH to study proteins in biological cells. The fluorescent proteins ECFP and EYFP, which are commonly used for dual-color studies in cells, have significant spectral cross talk. We will discuss the resolvability of these fluorescent proteins and present data that successfully resolve the protein mixtures in vitro and in vivo. Our results show that dual color PCH is a promising technique for the characterization of protein-protein interactions in intact cells.
机译:双色荧光相关光谱(FCS)和双光子激发相结合是探测蛋白质-蛋白质相互作用的有力工具。该技术的亚微米分辨率和单分子敏感性使其对体内应用具有吸引力。但是,大多数荧光染料混合物的两个发射通道之间的强光谱串扰为双色FCS实验分析提出了挑战。我们描述了一种新技术,即双色光子计数直方图(PCH)分析,它克服了与光谱串扰相关的一些挑战。双色PCH是常规PCH的扩展,可以同时分析两个检测通道的光子计数。我们证明了双色PCH在体外定量解析蛋白质混合物。我们还应用双色PCH来研究生物细胞中的蛋白质。通常用于细胞双色研究的荧光蛋白ECFP和EYFP具有明显的光谱串扰。我们将讨论这些荧光蛋白的可分辨性,并提供成功解决体外和体内蛋白混合物的数据。我们的结果表明,双色PCH是用于鉴定完整细胞中蛋白质与蛋白质相互作用的有前途的技术。

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