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Internally labeled Cy3/Cy5 DNA constructs show greatly enhanced photo-stability in single-molecule FRET experiments

机译:内部标记的Cy3 / Cy5 DNA构建体在单分子FRET实验中显示出大大增强的光稳定性

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摘要

DNA constructs labeled with cyanine fluorescent dyes are important substrates for single-molecule (sm) studies of the functional activity of protein–DNA complexes. We previously studied the local DNA backbone fluctuations of replication fork and primer–template DNA constructs labeled with Cy3/Cy5 donor–acceptor Förster resonance energy transfer (FRET) chromophore pairs and showed that, contrary to dyes linked ‘externally’ to the bases with flexible tethers, direct ‘internal’ (and rigid) insertion of the chromophores into the sugar-phosphate backbones resulted in DNA constructs that could be used to study intrinsic and protein-induced DNA backbone fluctuations by both smFRET and sm Fluorescent Linear Dichroism (smFLD). Here we show that these rigidly inserted Cy3/Cy5 chromophores also exhibit two additional useful properties, showing both high photo-stability and minimal effects on the local thermodynamic stability of the DNA constructs. The increased photo-stability of the internal labels significantly reduces the proportion of false positive smFRET conversion ‘background’ signals, thereby simplifying interpretations of both smFRET and smFLD experiments, while the decreased effects of the internal probes on local thermodynamic stability also make fluctuations sensed by these probes more representative of the unperturbed DNA structure. We suggest that internal probe labeling may be useful in studies of many DNA–protein interaction systems.
机译:花菁荧光染料标记的DNA构建体是蛋白质-DNA复合物功能活性单分子(sm)研究的重要底物。我们先前研究了用Cy3 / Cy5供体-受体福斯特共振能转移(FRET)生色团标记的复制叉和引物-模板DNA结构的局部DNA骨架波动,并表明,与染料“外部”连接至碱基的柔韧性相反系链,发色团直接“内部”(和刚性)插入糖-磷酸盐骨架中,从而导致DNA构建体可用于通过smFRET和sm荧光线性二向色性(smFLD)研究内在的和蛋白质诱导的DNA骨架波动。在这里,我们表明这些刚性插入的Cy3 / Cy5发色团还表现出两个附加的有用特性,显示出高的光稳定性和对DNA构建体局部热力学稳定性的最小影响。内部标记物提高的光稳定性显着降低了假阳性smFRET转换“背景”信号的比例,从而简化了对smFRET和smFLD实验的解释,而内部探针对局部热力学稳定性的降低影响也使波动感这些探针更能代表不受干扰的DNA结构。我们建议内部探针标记可能在许多DNA-蛋白质相互作用系统的研究中很有用。

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