清脆的
核酸
核酸检测
DNA
计算生物学
核糖核酸
生物
Cas9
核酸定量
化学
遗传学
基因
作者
Weiran Su,Junru Li,Ji Chen,Congshuo Chen,Yuzheng Wang,Huili Dai,Fengqin Li,Peifeng Liu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-03-20
卷期号:16 (7): 9940-9953
被引量:29
标识
DOI:10.1007/s12274-023-5567-4
摘要
Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) systems are becoming powerful tools for disease biomarkers detection. Due to the specific recognition, cis-cleavage and nonspecific trans-cleavage capabilities, CRISPR/Cas systems have implemented the detection of nucleic acid targets (DNA and RNA) as well as non-nucleic acid targets (e.g., proteins, exosomes, cells, and small molecules). In this review, we first summarize the principles and characteristics of various CRISPR/Cas systems, including CRISPR/Cas9, Cas12, Cas13 and Cas14 systems. Then, various types of applications of CRISPR/Cas systems used in detecting nucleic and non-nucleic acid targets are introduced emphatically. Finally, the prospects and challenges of their applications in biosensing are discussed.
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