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荧光铜纳米簇作为用于DNA甲基转移酶活性分析和抑制剂筛选的纳米染料

Fluorescent copper nanoclusters as a nano-dye for DNA methyltransferase activity analysis and inhibitor screening.

作者信息

Gao Dengpeng, Zhang Hongyue, Xu Yafei, Liu Yun, Xu Huiying, Cui Jianguo

机构信息

Department of General Surgery, Langfang People's Hospital, Langfang, 065000, China.

Department of Nursing, Bazhou City Hospital of Traditional, Bazhou, 065000, China.

出版信息

Anal Biochem. 2018 Oct 15;559:5-10. doi: 10.1016/j.ab.2018.08.011. Epub 2018 Aug 16.

Abstract

Fluorescent copper nanoslusters (CuNCs) as a new class of fluorophores have attracted more and more attention due to their ease of synthesis, excellent optical properties, and low cost. In this study, a novel label-free fluorescent method was developed for the detection of DNA methyltransferases based on template length-dependent of dsDNA-CuNCs. In the absence of DNA adenine methylation methyltransferase (Dam MTase), the dsDNA containing the methylation-responsive sequence could effectively template the formation of fluorescent CuNCs with bright fluorescence. When the dsDNA substrate is methylated by Dam MTase, the methylation-sensitive restriction endonuclease Dpn I cleaves the methylated dsDNA and produces shorter dsDNA product, which fails to template fluorescent CuNCs. So, the Dam MTase activity could be identified by the changes of CuNCs' fluorescence. Based on this method, a linear range of 0.5-10 U/mL was achieved with high sensitivity and selectivity. Moreover, we also demonstrate the proposed method can be applied to evaluation and screening of inhibitors for Dam MTase.

摘要

荧光铜纳米簇(CuNCs)作为一类新型荧光团,因其易于合成、优异的光学性能和低成本而受到越来越多的关注。在本研究中,基于双链DNA-CuNCs的模板长度依赖性,开发了一种用于检测DNA甲基转移酶的新型无标记荧光方法。在不存在DNA腺嘌呤甲基转移酶(Dam MTase)的情况下,含有甲基化响应序列的双链DNA可以有效地模板化形成具有明亮荧光的荧光CuNCs。当双链DNA底物被Dam MTase甲基化时,甲基化敏感的限制性内切酶Dpn I切割甲基化的双链DNA并产生较短的双链DNA产物,该产物无法模板化荧光CuNCs。因此,Dam MTase活性可以通过CuNCs荧光的变化来鉴定。基于该方法,实现了0.5-10 U/mL的线性范围,具有高灵敏度和选择性。此外,我们还证明了所提出的方法可用于评估和筛选Dam MTase的抑制剂。

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