Dong Zhen-Zhen, Zhang Lin, Qiao Min, Ge Jia, Liu Ai-Ling, Li Zhao-Hui
College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450001, PR China.
College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450001, PR China.
Talanta. 2016;146:253-8. doi: 10.1016/j.talanta.2015.08.055. Epub 2015 Aug 28.
DNA 3'-phosphatase takes an important role in DNA damage repair, replication and recombination. Here, we present a novel label-free fluorescent assay for T4 polynucleotide kinase/phosphatase (T4 PNKP) activity and its inhibitor screening by using poly(thymine)-templated fluorescent copper nanoparticles (CuNPs) as a fluorescent indicator. In this assay, we designed a simple T-rich hairpin primer with a 3'-phosphoryl end, which can serve as both the substrate for T4 PNKP and DNA template for the formation of fluorescent CuNPs. Once the phosphorylated hairpin primer was hydrolyzed by T4 PNKP, the resulting hairpin primer with a 3'-hydroxyl end was immediately elongated to form a long double-strand product by DNA polymerase, which prohibited the formation of fluorescent CuNPs due to the lack of poly T single-stranded DNA template. This new strategy provides a sensitive, selective, and cost-effective manner for T4 PNKP analysis, which holds a great potential in the study of DNA damage repair mechanisms.
DNA 3'-磷酸酶在DNA损伤修复、复制和重组过程中发挥着重要作用。在此,我们提出了一种新颖的无标记荧光测定法,用于检测T4多核苷酸激酶/磷酸酶(T4 PNKP)的活性及其抑制剂筛选,该方法使用聚胸腺嘧啶模板化荧光铜纳米颗粒(CuNPs)作为荧光指示剂。在该测定法中,我们设计了一种带有3'-磷酸化末端的简单富含胸腺嘧啶的发夹引物,它既可以作为T4 PNKP的底物,又可以作为形成荧光CuNPs的DNA模板。一旦磷酸化的发夹引物被T4 PNKP水解,产生的带有3'-羟基末端的发夹引物会立即被DNA聚合酶延伸形成长双链产物,由于缺乏聚T单链DNA模板,这会阻止荧光CuNPs的形成。这种新策略为T4 PNKP分析提供了一种灵敏、选择性高且经济高效的方法,在DNA损伤修复机制的研究中具有巨大潜力。