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Tracking of Single Quantum Dot Labeled EcoRV Sliding along DNA Manipulated by Double Optical Tweezers

机译:单量子点标记的EcoRV沿双光学镊子操纵的DNA滑动的跟踪。

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摘要

Fluorescence microscopy provides a powerful method to directly observe single enzymes moving along a DNA held in an extended conformation. In this work, we present results from single EcoRV enzymes labeled with quantum dots which interact with DNA manipulated by double optical tweezers. The application of quantum dots facilitated accurate enzyme tracking without photobleaching whereas the tweezers allowed us to precisely control the DNA extension. The labeling did not affect the biochemical activity of EcoRV checked by directly observing DNA digestion on the single molecule level. We used this system to demonstrate that during sliding, the enzyme stays in close contact with the DNA. Additionally, slight overstretching of the DNA resulted in a significant decrease of the 1D diffusion constant, which suggests that the deformation changes the energy landscape of the sliding interaction. Together with the simplicity of the setup, these results demonstrate that the combination of optical tweezers with fluorescence tracking is a powerful tool for the study of enzyme translocation along DNA.
机译:荧光显微术提供了一种强大的方法,可以直接观察沿扩展构象保持的DNA的单个酶的运动。在这项工作中,我们介绍了单个量子点标记的EcoRV酶的结果,该量子点与由双光镊操纵的DNA相互作用。量子点的应用促进了酶的精确跟踪而没有光漂白,而镊子使我们能够精确地控制DNA的延伸。通过直接观察单分子水平的DNA消化,标记不会影响EcoRV的生化活性。我们使用该系统来证明在滑动过程中,酶与DNA保持紧密接触。此外,DNA的过度拉伸会导致1D扩散常数显着降低,这表明变形会改变滑动相互作用的能级。连同设置的简单性,这些结果表明,光镊与荧光跟踪的组合是研究酶沿DNA转运的强大工具。

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