Key Laboratory of Laboratory Medical Diagnostics of Education, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, PR China.
Key Laboratory of Laboratory Medical Diagnostics of Education, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, PR China.
Anal Chim Acta. 2021 Jan 25;1143:157-165. doi: 10.1016/j.aca.2020.11.043. Epub 2020 Nov 30.
Sensitive and specific miRNA detection is essential for the early cancer diagnosis. In this work, we design a fluorescent microRNA biosensor based on exponential amplification reaction (EXPAR) and nicking endonuclease-powered three-dimensional (3-D) bipedal DNA walkers (BDW). Target microRNA initiates EXPAR with the help of polymerase and nicking endonuclease to generate the large number of BDW in solution. The newly generated BDW can be continuously assembled onto polystyrene microsphere track co-modified with fluorescence-labeled DNA strand. Thus, in the presence of nicking endonuclease, the walking machine is activated to produce enhanced fluorescent signal in the supernatant. Besides, we prove that BDW holds the faster walking speed than single-legged DNA walker (SDW) based on comparative study. Under optimal conditions, the proposed amplification method owns a wide linear range from 10 fM to 5 nM with a detection limit down to 5.2 fM. The reaction time of the assay takes about 70 min. The combination of enzyme-assisted EXPAR in solution and enzyme-powered BDW on particle significantly increases the signal amplification efficiency and improves the detection sensitivity. Therefore, our method has enormous potential for the application of BDW-related biosensors.
灵敏和特异的 miRNA 检测对于癌症的早期诊断至关重要。在本工作中,我们设计了一种基于指数扩增反应(EXPAR)和切口酶驱动的三维(3-D)双足 DNA walker(BDW)的荧光 miRNA 生物传感器。靶 miRNA 在聚合酶和切口酶的帮助下启动 EXPAR,以在溶液中生成大量的 BDW。新生成的 BDW 可以连续组装到聚苯乙烯微球轨道上,该轨道同时修饰有荧光标记的 DNA 链。因此,在存在切口酶的情况下,行走机器被激活,在上清液中产生增强的荧光信号。此外,我们通过比较研究证明 BDW 比单腿 DNA walker(SDW)具有更快的行走速度。在最佳条件下,所提出的扩增方法具有从 10 fM 到 5 nM 的宽线性范围,检测限低至 5.2 fM。测定的反应时间约为 70 分钟。溶液中酶辅助的 EXPAR 和颗粒上酶驱动的 BDW 的结合显著提高了信号放大效率,提高了检测灵敏度。因此,我们的方法在 BDW 相关生物传感器的应用中具有巨大的潜力。