反式激活crRNA
清脆的
电极
纳米技术
检出限
电化学
核酸
电化学气体传感器
DNA
化学
组合化学
色谱法
材料科学
Cas9
生物化学
基因
物理化学
作者
Бо Лю,Weishen Lu,Yibo Huang,Xiaoru Zhang,Xunyi Yuan
标识
DOI:10.1016/j.snb.2024.135406
摘要
In recent years, electrochemical sensors for nucleic acid testing based on CRISPR/Cas12a technology have attracted widespread interest due to their ease of operation and high detection sensitivity. Here, a label-free electrochemical sensor amplified by primer exchange reaction (PER), hybridization chain reaction (HCR) and CRISPR/Cas12a system was developed for analyzing miRNA- 155 and PCB 77. In the presence of targets, PER was initiated, whose products could be used to trigger the trans-cleavage activity of Cas12a for the single-stranded DNA (ssDNA) on the electrode. Afterwards, with the amplification of HCR on the electrode and electrostatic adsorption of Ru(NH3)63+, the concentration of the targets could be indicated by the DPV intensity with a low background signal. The detection limits for miRNA- 155 and PCB 77 were estimated to be 67 aM and 6.9 pg/L, respectively. This work provides a versatile method for sensitive detection of different targets using the same crRNA and can be used in various biochemical investigations.
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