School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Chongqing Key Laboratory of Catalysis and New Environmental Materials, College of Environment and Resources, Chongqing Technology and Business University, Chongqing 400067, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2019 Mar 5;210:335-340. doi: 10.1016/j.saa.2018.11.048. Epub 2018 Nov 19.
A visual and sensitive Hg detection strategy was developed based on split DNAzyme amplification and hemin-graphene oxide composites (H-GNs). Two split DNAzyme sequences can form two entire enzyme-strands DNA (E-DNA) by T-Hg-T interaction. The E-DNA can bind with the loop of molecular beacon (MB) to form Mg-dependent DNAzyme structure. The formed DNAzyme can circularly cleave the loop of MB, resulting large amount of DNA fragments. The resultant DNA fragments can prevent H-GNs from aggregation by adsorbing on its surface. Consequently, the supernate with large amount of H-GNs shows dark blue color after chromogenic reaction. This strategy shows a linear range from 50 pM to 1200 pM. The limit detection can be low to 33 pM. This strategy provides a visual and enzyme-free amplification mode for quick and sensitive screen of Hg.
基于分裂 DNA zyme 扩增和血红素-氧化石墨烯复合材料(H-GNs),开发了一种可视化和灵敏的 Hg 检测策略。两个分裂 DNA 酶序列可以通过 T-Hg-T 相互作用形成两个完整的酶链 DNA(E-DNA)。E-DNA 可以与分子信标(MB)的环结合,形成 Mg 依赖性 DNAzyme 结构。形成的 DNAzyme 可以循环切割 MB 的环,产生大量的 DNA 片段。所得的 DNA 片段可以通过吸附在其表面来防止 H-GNs 聚集。因此,显色反应后,含有大量 H-GNs 的上清液呈现深蓝色。该策略在 50 pM 至 1200 pM 的范围内呈线性,检测限低至 33 pM。该策略为快速灵敏地筛选 Hg 提供了可视化和无酶的扩增模式。