Huang Wan, Zhou Yue, Zhan Danyan, Lai Guosong
Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Chemical Engineering, Hubei Normal University, Huangshi, 435002, China.
Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Chemical Engineering, Hubei Normal University, Huangshi, 435002, China.
Anal Chim Acta. 2021 Apr 15;1154:338317. doi: 10.1016/j.aca.2021.338317. Epub 2021 Feb 11.
By the employment of a homogeneous biorecognition reaction to induce the assembled formation of DNA nanostructures at an electrode, herein we develop a novel biosensing method for the ultrasensitive electrochemical detection of kanamycin (Kana) antibiotic. A DNA complex consisting of Kana-aptamer and a hairpin DNA with an exposed 3'-end was first designed for conducting the homogeneous reaction with Kana in the presence of exonuclease I (Exo I). It resulted in the production of a hairpin DNA with a blunt terminus, which could be used for triggering the assembled formation of a layer of DNA nanostructures with orderly distribution and abundant biotin sites at a gold electrode. Then, high-content methylene blue and horseradish peroxidase (HRP)-functionalized gold nanotags would be captured onto the electrode to realize the electrocatalytic signal transduction. Due to the Exo I and HRP-assisted dual signal amplification, a very low detection limit of 9.1 fg mL was obtained for the Kana assay along with a very wide linear range over five-order of magnitude. Considering the excellent performance of the method, it exhibits a promising prospect for practical applications.
通过利用均相生物识别反应在电极上诱导DNA纳米结构的组装形成,我们在此开发了一种用于超灵敏电化学检测卡那霉素(Kana)抗生素的新型生物传感方法。首先设计了一种由卡那霉素适配体和具有暴露3'-末端的发夹DNA组成的DNA复合物,用于在外切核酸酶I(Exo I)存在下与卡那霉素进行均相反应。这导致产生具有平端的发夹DNA,其可用于触发在金电极上形成一层具有有序分布和丰富生物素位点的DNA纳米结构的组装。然后,高含量的亚甲蓝和辣根过氧化物酶(HRP)功能化的金纳米标签将被捕获到电极上以实现电催化信号转导。由于Exo I和HRP辅助的双信号放大,卡那霉素检测获得了9.1 fg mL的极低检测限以及超过五个数量级的非常宽的线性范围。考虑到该方法的优异性能,它在实际应用中展现出广阔的前景。