清脆的
生物传感器
小RNA
化学
纳米技术
计算生物学
材料科学
生物
生物化学
基因
作者
Xuefeng Wang,Fengyi Wang,Jianrong Wang,Yunqing Liu,Chaomin Gao,Shenguang Ge,Jinghua Yu
标识
DOI:10.1016/j.snb.2022.132480
摘要
Herein, based on CRISPR/Cas12a and catalytic hairpin assembly (CHA) non-enzyme amplification technology, a general photoelectrochemical (PEC) biosensor with high sensitivity and specificity is constructed using Bi/g-C3N4 nanohybrids as photoelectric composite electrode for the detection of miRNA-122. Notably, the single-strand DNA labelled with the sensitizer methylene blue (MB) was combined with the electrode to secondary improved the photocurrent response and effectively reduced the detection background. The miRNA-122 was specifically recognized by the CHA process, and then amplified into a rich signal output, which effectively improved the detection sensitivity. The target DNA complex generated by CHA cycle on the electrode surface hybridized with Cas12a-crRNA duplex to formed the Cas12a-crRNA-target DNA ternary complex, which activated their trans-cleavage ability and repelled MB to leave the electrode surface. The PEC signal was significantly reduced, achieving accurate detection of the miRNA-122. Under the action of multiple amplification mechanisms, the sensor showed prominent sensitivity and selectivity, the universal CRISPR/Cas12a cutting characteristics further expanded its analysis potential and simplified the operation difficulty, which can expand the application in biomedical detection and clinical diagnosis, showing great potential in efficient nucleic acid detection and in vitro diagnosis.
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