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Fluorescently labeled circular DNA molecules for DNA topology and topoisomerases

机译:荧光标记的环状DNA分子用于DNA拓扑和拓扑异构酶

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摘要

DNA topology plays essential roles in several fundamental biological processes, such as DNA replication, recombination, and transcription. Typically agarose gel electrophoresis is employed to study DNA topology. Since gel electrophoresis is time-consuming and labor intensive, it is desirable to develop other methods, such as fluorescence-based methods, for such studies. In this paper we report the synthesis of a type of unique fluorescence-labeled DNA molecules that can be used to study DNA topology and topoisomerases by fluorescence resonance energy transfer (FRET). Specifically, we inserted an 82 nt. synthetic DNA oligomer FL905 carrying a 42 nt. AT sequence with fluorescein and dabcyl labels into a gapped DNA molecule to generate relaxed and supercoiled pAB1_FL905. Since the fluorescence intensity of pAB1_FL905 is dependent on its supercoiling status, pAB1_FL905 is a powerful tool to study DNA topology and topoisomerases by FRET. pAB1_FL905 can also be developed into rapid and efficient high-throughput screening assays to identify inhibitors that target various DNA topoisomerases.
机译:DNA拓扑在几个基本的生物学过程中起着至关重要的作用,例如DNA复制,重组和转录。通常,琼脂糖凝胶电泳用于研究DNA拓扑。由于凝胶电泳既费时又费力,因此需要开发其他方法,例如基于荧光的方法进行此类研究。在本文中,我们报告了一种独特的荧光标记DNA分子的合成,该分子可用于通过荧光共振能量转移(FRET)研究DNA拓扑和拓扑异构酶。具体来说,我们插入了82nt。合成的DNA低聚物FL905,带有42nt。将带有荧光素和dabcyl标记的AT序列插入有缺口的DNA分子中,以产生松弛和超螺旋的pAB1_FL905。由于pAB1_FL905的荧光强度取决于其超螺旋状态,因此pAB1_FL905是研究FRET的DNA拓扑和拓扑异构酶的有力工具。 pAB1_FL905也可以发展成为快速有效的高通量筛选测定法,以鉴定靶向各种DNA拓扑异构酶的抑制剂。

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