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基于靶标触发的滚环扩增用于无标记和灵敏的荧光尿嘧啶-DNA 糖基化酶活性检测和抑制。

Target-triggered activation of rolling circle amplification for label-free and sensitive fluorescent uracil-DNA glycosylase activity detection and inhibition.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, PR China.

Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, PR China.

出版信息

Talanta. 2019 Nov 1;204:812-816. doi: 10.1016/j.talanta.2019.06.065. Epub 2019 Jun 19.

Abstract

The expression variations of uracil-DNA glycosylase (UDG) can be used as effective biomarkers for the evaluation of gene regulation and related diseases. Here, by using a new target-triggered activation of rolling circle amplification (RCA) signal enhancement strategy, we have established a sensitive and label-free fluorescent approach for UDG activity detection and inhibition. The target UDG specifically recognizes and excises the uracil bases in a three-strand containing DNA complex to liberate one of the strands. Subsequent ligation of the excised DNA complex converts it into a suitable primer/circular template structure for the initiation of RCA for the generation of long DNA sequences with many repeated G-quadruplexes. Protoporphyrin IX further binds these G-quadruplexes to show substantially enhanced fluorescence to achieve sensitive detecting the activity of UDG with the detection limit as low as 0.00014 U mL. Besides, this assay approach has a high specificity toward UDG and can also be utilized to evaluate its inhibition by the uracil glycosylase inhibitor, highlighting the promising applications for convenient and sensitive UDG activity detection and inhibition for disease diagnosis and drug screening.

摘要

尿嘧啶-DNA 糖基化酶 (UDG) 的表达变化可用作评估基因调控和相关疾病的有效生物标志物。在这里,我们使用一种新的基于目标触发的滚环扩增 (RCA) 信号增强策略,建立了一种用于 UDG 活性检测和抑制的灵敏、无标记的荧光方法。目标 UDG 特异性识别并切除三链体 DNA 复合物中的尿嘧啶碱基,释放其中一条链。随后,被切除的 DNA 复合物的连接将其转化为合适的引物/环形模板结构,用于 RCA 的起始,以生成具有许多重复 G-四链体的长 DNA 序列。原卟啉 IX 进一步结合这些 G-四链体,以显示出显著增强的荧光,从而实现对 UDG 活性的灵敏检测,检测限低至 0.00014 U/mL。此外,该测定方法对 UDG 具有高特异性,也可用于评估其被尿嘧啶糖基化酶抑制剂抑制的情况,突出了用于疾病诊断和药物筛选的方便、灵敏的 UDG 活性检测和抑制的应用前景。

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