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基于 G-四链体 DNA zyme 分子信标的双功能比色寡核苷酸探针。

Bifunctional colorimetric oligonucleotide probe based on a G-quadruplex DNAzyme molecular beacon.

机构信息

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, P. R. China.

出版信息

Anal Chem. 2011 Dec 1;83(23):8871-6. doi: 10.1021/ac2006763. Epub 2011 Nov 3.

Abstract

A label-free bifunctional colorimetric oligonucleotide probe for DNA and protein detection has been developed on the basis of a novel catalytic molecular beacon consisting of two hairpin structures and a split G-quadruplex DNAzyme in the middle. The two loops of this molecular beacon consist of thrombin aptamer sequence and the complementary sequence of target DNA, which are utilized to sense single-stranded DNA and thrombin. The G-quadruplex DNAzyme can effectively catalyze the H(2)O(2)-mediated oxidation of 3,3',5,5'-tetramethylbenzidine sulfate to generate colorimetric signal. Upon addition of the target, the DNA or protein combines with one loop of the hairpin structures, and meanwhile drives the middle G-quadruplex DNAzyme to dissociate. This results in a decrease of catalytic activity, enabling the separate analysis of DNA and thrombin.

摘要

一种无标记双功能比色寡核苷酸探针已被开发用于 DNA 和蛋白质检测,其基础是一种新型催化分子信标,该信标由两个发夹结构和中间的分裂 G-四链体 DNA 酶组成。该分子信标的两个环由凝血酶适体序列和靶 DNA 的互补序列组成,用于感测单链 DNA 和凝血酶。G-四链体 DNA 酶可有效催化 H(2)O(2)介导的 3,3',5,5'-四甲基联苯胺硫酸盐的氧化,生成比色信号。加入靶标后,DNA 或蛋白质与发夹结构的一个环结合,同时驱动中间的 G-四链体 DNA 酶解离。这导致催化活性降低,从而能够分别分析 DNA 和凝血酶。

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