Pharmacy College, Henan University of Chinese Medicine, Zhengzhou 450046, P. R. China.
School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, P. R. China.
Analyst. 2019 Oct 7;144(19):5691-5699. doi: 10.1039/c9an01266d. Epub 2019 Sep 11.
Herein, a novel aptasensor was constructed for ultrasensitive detection of bisphenol A (BPA). In this method, an electrochemically mediated atom transfer radical polymerization (eATRP) signal amplification strategy was applied to BPA detection for the first time. The 5'-end modified sulfhydryl group and the 3'-end modified azide group hairpin DNA were immobilized on a gold electrode through an Au-S bond. The double-stranded DNA was formed by the hybridization of an aptamer and a single-stranded DNA partially paired with the hairpin DNA. In the presence of BPA, the aptamer combined with BPA and the single-stranded DNA was released to open the hairpin structure, making the azide groups at the 3' end exposed. Subsequently the initiator of eATRP was introduced into hairpin DNA through click chemistry reaction and eATRP was conducted for the polymerization of the electroactive probe ferrocene methyl methacrylate (FMMA). As a result, the ultrasensitive detection of BPA was realized, and the detection limit of this aptasensor was as low as 59 aM and a good selectivity was obtained in the presence of 100-fold structural analogs. The application of this aptasensor was evaluated by detecting BPA in pure water samples, and recoveries were in the range of 95.23-98.40%, holding promising applications in biological analysis.
本文构建了一种用于检测双酚 A (BPA) 的新型适体传感器。在该方法中,首次将电化学介导的原子转移自由基聚合 (eATRP) 信号放大策略应用于 BPA 的检测。巯基修饰的 5'端和叠氮基修饰的 3'端发夹 DNA 通过 Au-S 键固定在金电极上。通过适体与部分与发夹 DNA 配对的单链 DNA 的杂交形成双链 DNA。在存在 BPA 的情况下,适体与 BPA 结合并释放单链 DNA 以打开发夹结构,使 3'端的叠氮基团暴露。随后,通过点击化学反应将 eATRP 的引发剂引入到发夹 DNA 中,并进行电活性探针二茂铁甲基丙烯酸甲酯 (FMMA) 的聚合。因此,实现了对 BPA 的超灵敏检测,该适体传感器的检测限低至 59 aM,并且在存在 100 倍结构类似物的情况下获得了良好的选择性。该适体传感器的应用通过在纯水样品中检测 BPA 进行了评估,回收率在 95.23-98.40%范围内,在生物分析中具有广阔的应用前景。