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用于 DNA 拓扑结构和拓扑异构酶的荧光标记环形 DNA 分子。

Fluorescently labeled circular DNA molecules for DNA topology and topoisomerases.

机构信息

Biomolecular Science Institute, Florida International University, Miami, FL 33199.

Department of Chemistry &Biochemistry, Florida International University, Miami, FL 33199.

出版信息

Sci Rep. 2016 Oct 31;6:36006. doi: 10.1038/srep36006.

Abstract

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.

摘要

DNA 拓扑结构在多个基本生物学过程中发挥着重要作用,例如 DNA 复制、重组和转录。通常采用琼脂糖凝胶电泳来研究 DNA 拓扑结构。由于凝胶电泳耗时且劳动强度大,因此人们希望开发其他方法,如荧光法,用于此类研究。在本文中,我们报告了一种独特的荧光标记 DNA 分子的合成方法,该分子可用于通过荧光共振能量转移(FRET)研究 DNA 拓扑结构和拓扑异构酶。具体而言,我们将携带荧光素和 dabcyl 标记的 82nt 合成 DNA 寡核苷酸 FL905 插入到缺口 DNA 分子中,以生成松弛和超螺旋 pAB1_FL905。由于 pAB1_FL905 的荧光强度取决于其超螺旋状态,因此 pAB1_FL905 是通过 FRET 研究 DNA 拓扑结构和拓扑异构酶的有力工具。pAB1_FL905 还可以开发成快速高效的高通量筛选测定法,以鉴定针对各种 DNA 拓扑异构酶的抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db53/5087112/9ad67efcc3f7/srep36006-f1.jpg

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