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Quantitative fluorescence resonance energy transfer measurements using microarray technology

机译:使用微阵列技术的定量荧光共振能量转移测量

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摘要

Fluorescence resonance energy transfer (FRET) has found wide use in structural biology, biochemistry, and cell biology for measuring intra- and inter-molecular distances in the 1-10 nm range and for obtaining quantitative spatial and temporal information about the interaction of proteins, lipids, and DNA. The measurements of distances and interactions are based on the calculation of the fluorescence transfer efficiency using some algorithms to process the acquired images from several different filter sets. However, FRET measurements can suffer from several sources of distortion because of cross talk between donor and acceptor fluorophores. In this paper, we measured the FRET efficiency on glass coverslips using microarray technology and described an algorithm to analyze the FRET data obtained, which is corrected for the cross talk due to spectral overlap of donor and acceptor molecules. Measurement of the interaction of the donor and acceptor, which are mixed together or coupled to the respective 3'-end and 5'-end of a single-strand DNA are shown to document the accuracy of the approach, and allow one to estimate cross talk between the different filter units and to reveal the relationship of the FRET efficiencies of these two samples relative to the donor and acceptor concentrations.
机译:荧光共振能量转移(FRET)已广泛用于结构生物学,生物化学和细胞生物学中,用于测量1-10 nm范围内的分子内和分子间距离,以及获得有关蛋白质相互作用的定量时空信息,脂质和DNA。距离和相互作用的测量基于荧光转移效率的计算,使用一些算法来处理从多个不同滤镜组获取的图像。但是,由于供体和受体荧光团之间的串扰,FRET测量可能会受到多种失真的影响。在本文中,我们使用微阵列技术测量了玻璃盖玻片上的FRET效率,并描述了一种用于分析获得的FRET数据的算法,该算法针对因供体和受体分子的光谱重叠而引起的串扰进行了校正。显示了供体和受体的相互作用的测量结果,供体和受体混合在一起或耦合到单链DNA的相应3'端和5'端,可以证明该方法的准确性,并允许人们估计交叉讨论不同过滤器单元之间的关系,以揭示这两个样品的FRET效率相对于供体和受体浓度的关系。

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