Key Laboratory of Chemical Sensing & Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China.
School of Biological Sciences and Technology, University of Jinan, Jinan 250022, PR China.
Biosens Bioelectron. 2016 Jan 15;75:315-9. doi: 10.1016/j.bios.2015.08.031. Epub 2015 Aug 18.
In this work, a simple, label-free, low cost electrochemical biosensor for highly sensitive and selective detection of Escherichia coli has been developed on the basis of rolling circle amplification (RCA) coupled peroxidase-mimicking DNAzyme amplification. A aptamer-primer probe (APP) containing anti-E. coli aptamer and a primer sequence complementary to a circular probe, which includes two G-quadruplex units, is used for recognizing target and triggering RCA-based polymerase elongation. Due to RCA coupled DNAzyme amplification strategy, the presence of target E. coli leads to the formation of numerous G-quadruplex oligomers on electrode, which folds into G-quadruplex/hemin complexs with the help of K(+) and hemin, thus generating extremely strong catalytic activity toward H2O2 and giving a remarkably strong electrochemical response. As far as we know, this work is the first time that RCA coupled peroxidase-mimicking DNAzyme amplification technique have been integrated into electrochemical assay for detecting pathogenic bacteria. Under optimal conditions, the proposed biosensor exhibits ultrahigh sensitivity toward E. coli with detection limits of 8cfumL(-1) and a detection range of 5 orders of magnitude. Besides, our biosensor also shows high selectivity toward target E. coli and has the advantages in its rapidness, low cost, simplified operations without the need of electrochemical labeling steps and additional labile reagents. Hence, the RCA coupled peroxidase-mimicking DNAzyme amplification-based electrochemical method might create a useful and practical platform for detecting E. coli and related food safety analysis and clinical diagnosis.
在这项工作中,基于滚环扩增(RCA)偶联过氧化物酶模拟 DNA 酶扩增,开发了一种简单、无标记、低成本的电化学生物传感器,用于高灵敏度和选择性检测大肠杆菌。含有抗大肠杆菌适体和与包含两个 G-四链体单元的圆形探针互补的引物序列的适体-引物探针(APP)用于识别靶标并触发基于 RCA 的聚合酶延伸。由于 RCA 偶联的 DNA 酶扩增策略,靶标大肠杆菌的存在导致在电极上形成许多 G-四链体寡聚物,这些寡聚物在 K(+)和血红素的帮助下折叠成 G-四链体/血红素复合物,从而对 H2O2 产生极强的催化活性,并产生非常强的电化学响应。据我们所知,这是首次将 RCA 偶联过氧化物酶模拟 DNA 酶扩增技术集成到用于检测致病菌的电化学分析中。在最佳条件下,该生物传感器对大肠杆菌具有超高的灵敏度,检测限为 8cfumL(-1),检测范围为 5 个数量级。此外,我们的生物传感器对靶标大肠杆菌也具有高选择性,并且具有快速、低成本、操作简单的优点,无需电化学标记步骤和额外的不稳定试剂。因此,基于 RCA 偶联过氧化物酶模拟 DNA 酶扩增的电化学方法可能为检测大肠杆菌及相关食品安全分析和临床诊断创建一个有用且实用的平台。