Xie Shunbi, Chai Yaqin, Yuan Yali, Bai Lijuan, Yuan Ruo
Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Anal Chim Acta. 2014 Jun 17;832:51-7. doi: 10.1016/j.aca.2014.04.065. Epub 2014 May 2.
In this work, a new signal amplified strategy was constructed based on isothermal exponential amplification reaction (EXPAR) and hybridization chain reaction (HCR) generating the hemin/G-quadruplex horseradish peroxidase-mimicking DNAzyme (HRP-mimicking DNAzyme) nanowires as signal output component for the sensitive detection of thrombin (TB). We employed EXPAR's ultra-high amplification efficiency to produce a large amount of two hairpin helper DNAs within a minutes. And then the resultant two hairpin helper DNAs could autonomously assemble the hemin/G-quadruplex HRP-mimicking DNAzymes nanowires as the redox-active reporter units on the electrode surface via hybridization chain reaction (HCR). The hemin/G-quadruplex structures simultaneously served as electron transfer medium and electrocatalyst to amplify the signal in the presence of H2O2. Specifically, only when the EXPAR reaction process has occurred, the HCR could be achieved and the hemin/G-quadruplex complexes could be formed on the surface of an electrode to give a detectable signal. The proposed strategy combines the amplification power of the EXPAR, HCR, and the inherent high sensitivity of the electrochemical detection. With such design, the proposed assay showed a good linear relationship within the range of 0.1 pM-50 nM with a detection limit of 33 fM (defined as S/N=3) for TB.
在本研究中,基于等温指数扩增反应(EXPAR)和杂交链式反应(HCR)构建了一种新的信号放大策略,生成血红素/ G-四链体模拟辣根过氧化物酶的DNAzyme(HRP模拟DNAzyme)纳米线作为信号输出组件,用于灵敏检测凝血酶(TB)。我们利用EXPAR的超高扩增效率在数分钟内产生大量的两种发夹型辅助DNA。然后,所得到的两种发夹型辅助DNA可通过杂交链式反应(HCR)在电极表面自主组装成血红素/ G-四链体模拟HRP的DNAzyme纳米线,作为氧化还原活性报告单元。在H2O2存在下,血红素/ G-四链体结构同时作为电子转移介质和电催化剂来放大信号。具体而言,只有当EXPAR反应过程发生时,才能实现HCR,并且血红素/ G-四链体复合物才能在电极表面形成以给出可检测信号。所提出的策略结合了EXPAR、HCR的放大能力以及电化学检测固有的高灵敏度。通过这种设计,所提出的检测方法在0.1 pM - 50 nM范围内显示出良好的线性关系,对TB的检测限为33 fM(定义为S/N = 3)。