Ma Hongmin, Guo Bin, Yan Xiaoyu, Wang Tong, Que Haiying, Gan Xiufeng, Liu Ping, Yan Yurong
Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), College of Laboratory Medicine, Chongqing Medical University Chongqing 400016 China
RSC Adv. 2019 Jun 20;9(34):19347-19353. doi: 10.1039/c9ra02401h. eCollection 2019 Jun 19.
Nucleic acid analysis plays an important role in the diagnosis of diseases. There is a continuous demand to develop rapid and sensitive methods for the specific detection of nucleic acids. Herein, we constructed a highly sensitive and rapid fluorescent biosensor for the detection of BRCA1 by coupling a 3D DNA walker machine with spontaneous entropy-driven strand displacement reactions (ESDRs). In this study, the 3D DNA walker machine was well activated by the target DNA; this resulted in the cyclic utilization of the target DNA and the release of intermediate DNAs. Subsequently, the free intermediate DNAs triggered the circulation process of ESDRs with the help of the assistant probe A, leading to a significant enhancement of the fluorescence intensity. Due to the robust execution of the 3D DNA walker machine and highly efficient amplification capability of ESDRs, the developed biosensing method shows a wide linear range from 0.1 pM to 10 nM with the detection limit as low as 41.44 fM (S/N = 3). Moreover, the constructed biosensor displays superior specificity and has been applied to monitor BRCA1 in complex matrices. Thus, this elaborated cascade amplification biosensing strategy provides a potential platform for the bioassays of nucleic acids and the clinical diagnosis of diseases.
核酸分析在疾病诊断中发挥着重要作用。人们一直有开发快速灵敏的核酸特异性检测方法的需求。在此,我们通过将三维DNA步行机与自发熵驱动的链置换反应(ESDRs)相结合,构建了一种用于检测BRCA1的高灵敏快速荧光生物传感器。在本研究中,三维DNA步行机被目标DNA很好地激活;这导致目标DNA的循环利用和中间DNA的释放。随后,游离的中间DNA在辅助探针A的帮助下触发ESDRs的循环过程,导致荧光强度显著增强。由于三维DNA步行机的稳健运行和ESDRs的高效扩增能力,所开发的生物传感方法显示出从0.1 pM到10 nM的宽线性范围,检测限低至41.44 fM(S/N = 3)。此外,构建的生物传感器具有优异的特异性,并已应用于复杂基质中BRCA1的监测。因此,这种精心设计的级联放大生物传感策略为核酸生物分析和疾病临床诊断提供了一个潜在的平台。