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Visualization of Surface-tethered Large DNA Molecules with a Fluorescent Protein DNA Binding Peptide

机译:带有荧光蛋白DNA结合肽的表面束缚的大DNA分子的可视化

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摘要

Large DNA molecules tethered on the functionalized glass surface have been utilized in polymer physics and biochemistry particularly for investigating interactions between DNA and its binding proteins. Here, we report a method that uses fluorescent microscopy for visualizing large DNA molecules tethered on the surface. First, glass coverslips are biotinylated and passivated by coating with biotinylated polyethylene glycol, which specifically binds biotinylated DNA via avidin protein linkers and significantly reduces undesirable binding from non-specific interactions of proteins or DNA molecules on the surface. Second, the DNA molecules are biotinylated by two different methods depending on their terminals. The blunt ended DNA is tagged with biotinylated dUTP at its 3' hydroxyl terminus, by terminal transferase, while the sticky ended DNA is hybridized with biotinylated complimentary oligonucleotides by DNA ligase. Finally, a microfluidic shear flow makes single DNA molecules stretch to their full contour lengths after being stained with fluorescent protein-DNA binding peptide (FP-DBP).
机译:束缚在功能化玻璃表面上的大型DNA分子已用于高分子物理学和生物化学中,尤其是用于研究DNA及其结合蛋白之间的相互作用。在这里,我们报告了一种使用荧光显微技术可视化束缚在表面上的大型DNA分子的方法。首先,玻璃盖玻片被生物素化并通过涂有生物素化聚乙二醇而钝化,该聚乙二醇通过亲和素蛋白接头特异性结合生物素化DNA,并显着减少了蛋白质或DNA分子在表面上的非特异性相互作用所造成的不良结合。其次,根据分子的末端,可以通过两种不同的方法对DNA分子进行生物素化。末端平末端的DNA通过末端转移酶在其3'羟基末端被生物素化的dUTP标记,而末端黏性的DNA通过DNA连接酶与生物素化的互补寡核苷酸杂交。最终,微流剪切流使单个DNA分子在被荧光蛋白-DNA结合肽(FP-DBP)染色后伸展至其完整轮廓长度。

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