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利用单链DNA结合蛋白的固有荧光快速检测DNA中的四重结构

Fast detection of quadruplex structure in DNA by the intrinsic fluorescence of a single-stranded DNA binding protein.

作者信息

Zhuang Xin-ying, Tang Jun, Hao Yu-hua, Tan Zheng

机构信息

Laboratory of Biochemistry and Biophysics, College of Life Sciences, Wuhan University, Wuhan 430072, PR China.

出版信息

J Mol Recognit. 2007 Sep-Oct;20(5):386-91. doi: 10.1002/jmr.847.

Abstract

Single-stranded guanine-rich (G-rich) DNA can fold into a four-stranded G-quadruplex structure and such structures are implicated in important biological processes and therapeutic applications. So far, bioinformatic analysis has identified up to several hundred thousand of putative quadruplex sequences in the genome of human and other animal. Given such a large number of sequences, a fast assay would be desired to experimentally verify the structure of these sequences. Here we describe a method that identifies the quadruplex structure by a single-stranded DNA binding protein from a thermoautotrophic archaeon. This protein binds single-stranded DNA in the unfolded, but not in the folded form. Upon binding to DNA, its fluorescence can be quenched by up to 70%. Formation of quadruplex greatly reduces fluorescence quenching in a K+-dependent manner. This structure-dependent quenching provides simple and fast detection of quadruplex in DNA at low concentration without DNA labelling.

摘要

富含鸟嘌呤的单链(G-富集)DNA可折叠成四链G-四链体结构,此类结构与重要的生物学过程和治疗应用有关。到目前为止,生物信息学分析已在人类和其他动物的基因组中鉴定出多达数十万条假定的四链体序列。鉴于有如此大量的序列,需要一种快速检测方法来通过实验验证这些序列的结构。在此,我们描述了一种通过来自嗜热自养古菌的单链DNA结合蛋白鉴定四链体结构的方法。该蛋白以未折叠形式而非折叠形式结合单链DNA。与DNA结合后,其荧光可被淬灭高达70%。四链体的形成以K+依赖的方式极大地降低了荧光淬灭。这种依赖于结构的淬灭提供了一种在不进行DNA标记的情况下简单快速检测低浓度DNA中四链体的方法。

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