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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >An electrochemical biosensor for microRNA-196a detection based on cyclic enzymatic signal amplification and template-free DNA extension reaction with the adsorption of methylene blue
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An electrochemical biosensor for microRNA-196a detection based on cyclic enzymatic signal amplification and template-free DNA extension reaction with the adsorption of methylene blue

机译:基于循环酶促信号扩增和无模板DNA延伸反应的MicroRNA-196A检测电化学生物传感器与亚甲基蓝吸附

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摘要

A simple and sensitive electrochemical biosensor was developed for microRNA-196a detection, which is of important diagnostic significance for pancreatic cancer. It was based on cyclic enzymatic signal amplification (CESA) and template-free DNA extension reaction. In the presence of microRNA-196a, duplex-specific nuclease (DSN) catalyzed the digestion of the 3'-PO4 terminated capture probe (CP), resulting in the target recycling amplification. Meanwhile, the 3'-OH terminal of CP was exposed. Then, template-free DNA extension reaction was triggered by terminal deoxynucleotidyl transferase (TdT), producing amounts of single-stranded DNA (ssDNA). After ssDNA absorbed numerous methylene blue (MB), an ultrasensitive electrochemical readout was obtained. Based on this dual amplification mechanism, the proposed biosensor exhibited a high sensitivity for detection of microRNA-196a down to 15 aM with a linear range from 0.05 fM to 50 pM. This biosensor displayed high specificity, which could discriminate target microRNAs from one base mismatched microRNAs. It also showed good reproducibility and stability. Furthermore, it was successfully applied to the determination of microRNA-196a in plasma samples. In conclusion, with the excellent analytical performance, this biosensor might have the potential for application in clinical diagnostics of pancreatic cancer.
机译:为MicroRNA-196A检测开发了一种简单敏感的电化学生物传感器,这对于胰腺癌具有重要的诊断意义。它基于环状酶促信号扩增(CESA)和无模板的DNA延伸反应。在MicroRNA-196a的存在下,双相特异性核酸酶(DSN)催化了3'-PO4终止捕获探针(CP)的消化,导致目标再循环扩增。同时,CP的3'-OH末端暴露。然后,通过末端脱氧核苷酸转移酶(TDT)触发无模板的DNA延伸反应,产生单链DNA(SSDNA)的量。在SSDNA吸收许多亚甲基蓝(MB)后,获得超细电化学读数。基于该双扩增机理,所提出的生物传感器对MicroRNA-196A检测至15μl的高灵敏度,线性范围为0.05 fm至50 pm。这种生物传感器显示出高的特异性,可以从一个基础的Micrativeed Micrornas区分目标微稻草。它还表现出良好的再现性和稳定性。此外,它成功地应用于血浆样品中microRNA-196a的测定。总之,随着优异的分析性能,这种生物传感器可能具有胰腺癌临床诊断中的应用。

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