Key Laboratory of Sensor Analysis of Tumor Marker, Ministry of Education, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Biosens Bioelectron. 2017 Aug 15;94:243-249. doi: 10.1016/j.bios.2017.03.015. Epub 2017 Mar 7.
In this work, a novel silver nanoclusters (AgNCs) were in situ synthesized and used as versatile electrochemiluminescence (ECL) and electrochemical (EL) signal probes for thrombin detection by using DNAzyme-assisted target recycling and hybridization chain reaction (HCR) multiple amplification strategy. The presence of target thrombin firstly opened the hairpin DNA, followed by DNAzyme-catalytic recycling cleavage of excess substrates, which could generate large number of substrate fragments (s1). Then these s1 fragments were captured by SH-DNA on the Au nanoparticle-modified electrode, which further triggered the subsequent HCR of the hairpin DNA probes (H1 and H2) to form the long dsDNA. The numerous AgNCs were thus in situ synthesized by incubation the dsDNA template (with cytosine-rich loop)-modified electrode in solution with AgNO and sodium borohydride. By integrating the DNAzyme recycling and HCR dual amplification strategy, the amount of AgNCs is dramatically enhanced, leading to substantially amplified ECL and electrochemical signals for sensitive thrombin detection. Importantly, this design introduces the novel AgNCs into versatile ECL and EL bioassays by multiple amplification strategy, thus it is promising to provide a highly sensitive platform for various target biomolecules.
在这项工作中,我们原位合成了一种新型的银纳米簇(AgNCs),并将其用作多功能电致化学发光(ECL)和电化学(EL)信号探针,用于通过 DNAzyme 辅助的靶标循环和杂交链式反应(HCR)多重扩增策略检测凝血酶。靶标凝血酶的存在首先打开发夹 DNA,随后 DNAzyme 催化循环切割过量的底物,从而产生大量的底物片段(s1)。然后,这些 s1 片段被修饰在 Au 纳米颗粒上的 SH-DNA 捕获,进一步引发发夹 DNA 探针(H1 和 H2)的后续 HCR,形成长双链 DNA。然后,将含有胞嘧啶丰富环的 dsDNA 模板修饰的电极在含有 AgNO 和硼氢化钠的溶液中孵育,从而原位合成大量的 AgNCs。通过整合 DNAzyme 循环和 HCR 双重扩增策略,AgNCs 的数量大大增加,导致 ECL 和电化学信号显著放大,从而实现了对凝血酶的灵敏检测。重要的是,该设计通过多重扩增策略将新型 AgNCs 引入多功能 ECL 和 EL 生物测定中,因此有望为各种靶标生物分子提供高灵敏度的平台。