Mao Yu, Chen Yongli, Li Song, Lin Shuo, Jiang Yuyang
Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
The Ministry-Province Jointly Constructed Base for State Key Lab-Shenzhen Key Laboratory of Chemical Biology, the Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055, China.
Sensors (Basel). 2015 Nov 9;15(11):28244-56. doi: 10.3390/s151128244.
A novel biosensing platform was developed by integrating an aptamer-based DNA biosensor with graphene oxide (GO) for rapid and facile detection of adenosine triphosphate (ATP, as a model target). The DNA biosensor, which is locked by GO, is designed to contain two sensing modules that include recognition site for ATP and self-replication track that yields the nicking domain for Nt.BbvCI. By taking advantage of the different binding affinity of single-stranded DNA, double-stranded DNA and aptamer-target complex toward GO, the DNA biosensor could be efficiently released from GO in the presence of target with the help of a complementary DNA strand (CPDNA) that partially hybridizes to the DNA biosensor. Then, the polymerization/nicking enzyme synergetic isothermal amplification could be triggered, leading to the synthesis of massive DNA amplicons, thus achieving an enhanced sensitivity with a wide linear dynamic response range of four orders of magnitude and good selectivity. This biosensing strategy expands the applications of GO-DNA nanobiointerfaces in biological sensing, showing great potential in fundamental research and biomedical diagnosis.
通过将基于适体的DNA生物传感器与氧化石墨烯(GO)集成,开发了一种新型生物传感平台,用于快速简便地检测三磷酸腺苷(ATP,作为模型靶标)。被GO锁定的DNA生物传感器被设计为包含两个传感模块,其中一个是ATP识别位点,另一个是产生Nt.BbvCI切口结构域的自我复制轨道。利用单链DNA、双链DNA和适体-靶标复合物对GO的不同结合亲和力,在与DNA生物传感器部分杂交的互补DNA链(CPDNA)的帮助下,DNA生物传感器可以在靶标存在时从GO中有效释放。然后,可以触发聚合/切口酶协同等温扩增,导致大量DNA扩增子的合成,从而实现增强的灵敏度,线性动态响应范围宽达四个数量级,且具有良好的选择性。这种生物传感策略扩展了GO-DNA纳米生物界面在生物传感中的应用,在基础研究和生物医学诊断中显示出巨大潜力。