CRISPR-Cas12a-assisted elimination of the non-specific signal from non-specific amplification in the Exponential Amplification Reaction

被引:9
|
作者
Niu, Chenqi [1 ,3 ]
Liu, Juewen [3 ]
Xing, Xinhui [1 ,2 ]
Zhang, Chong [1 ,2 ]
机构
[1] Tsinghua Univ, Inst Biochem Engn, Dept Chem Engn, MOE Key Lab Ind Biocatalysis, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Ctr Synthet & Syst Biol, Beijing 100084, Peoples R China
[3] Univ Waterloo, Waterloo Inst Nanotechnol, Dept Chem, 200 Univ Ave West, Waterloo, ON N2L 3G1, Canada
基金
中国国家自然科学基金;
关键词
EXPAR; CRISPR-Cas12a; Suppression; Non-specific amplification; miRNA detection; ISOTHERMAL AMPLIFICATION; SENSITIVE DETECTION; OFF-TARGET; SARS-COV-2;
D O I
10.1016/j.aca.2023.340998
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Non-specific amplification is a major problem in nucleic acid amplification resulting in false-positive results, especially for exponential amplification reactions (EXPAR). Although efforts were made to suppress the influence of non-specific amplification, such as chemical blocking of the template's 3 '-ends and sequence-independent weakening of template-template interactions, it is still a common problem in many conventional EXPAR reactions. In this study, we propose a novel strategy to eliminate the non-specific signal from non-specific amplification by integrating the CRISPR-Cas12a system into two-templates EXPAR. An EXPAR-Cas12a strategy named EXPCas was developed, where the Cas12a system acted as a filter to filter out non-specific amplificons in EXPAR, suppressing and eliminating the influence of non-specific amplification. As a result, the signal-tobackground ratio was improved from 1.3 to 15.4 using this method. With microRNA-21 (miRNA-21) as a target, the detection can be finished in 40 min with a LOD of 103 fM and no non-specific amplification was observed.
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页数:8
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