清脆的
核酸
核酸检测
计算生物学
生物传感器
纳米技术
检测点注意事项
环介导等温扩增
计算机科学
化学
DNA
生物
材料科学
基因
生物化学
免疫学
作者
Xiwei Zhuang,Xueqiong Yang,Bo Cao,Haiming Sun,Xiaoyan Lv,Chijia Zeng,Fugang Li,Bin Qu,H. Susan Zhou,Feiyun Cui,Qin Zhou
标识
DOI:10.1149/1945-7111/ac5cec
摘要
The CRISPR/Cas system has gained enormous attention for its excellent gene-editing capabilities. In recent years, the reported trans-cleavage activity of some Cas proteins, including Cas12, Cas13 and Cas14, has given the CRISPR/Cas system an increasingly powerful molecular diagnostic ability. When the CRISPR/Cas system is introduced into the field of electrochemical (EC) biosensor, it confers the high specificity to distinguish single base mismatches of nucleic acid, excellent sensitivity with the limit of detection as low as attomole range, and well meets the point-of-care testing (POCT) requirements of nucleic acid testing (NAT). In this review, we have briefly introduced the history and inherent advantages of the CRISPR/Cas system. The EC sensing platforms based on CRISPR/Cas systems have been compared with the classical fluorescence and colorimetric platforms. And the isothermal amplification strategies suitable for CRISPR/Cas system have been summarized. After that, we have highlighted the application of EC biosensor based on CRISPR/Cas system (EC-CRISPR) in the detection and identification of cancers, bacteria and viruses. Finally, the future prospects of EC-CRISPR have been proposed.
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