Three novel Cas12a orthologs with robust DNA cleavage activity suitable for nucleic acid detection

被引:3
|
作者
Liu, Xueping [1 ,2 ]
Qiu, Xiaotong [2 ]
Han, Lichao
Yue, Yuan [3 ]
Xu, Shuai
Li, Fang [4 ]
Yao, Jiang
Sun, Lina
Li, Zhenjun [1 ,2 ]
机构
[1] Wenzhou Med Univ, Sch Lab Med & Life Sci, Wenzhou 325035, Zhejiang, Peoples R China
[2] Chinese Ctr Dis Control & Prevent, Natl Inst Communicable Dis Control & Prevent, State Key Lab Infect Dis Prevent & Control, Beijing 102206, Peoples R China
[3] Ningxia Univ, Key Lab Minist Educ Conservat & Utilizat Special B, Yinchuan, Peoples R China
[4] Tibet Univ, Dept Med, Lhasa 850000, Tibet, Peoples R China
基金
中国国家自然科学基金;
关键词
CRISPR-Cas12a; DNA cleavage; Nucleic acid detection; Single -based resolution; CPF1; CLASSIFICATION;
D O I
10.1016/j.gene.2022.147055
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Developing rapid and accurate pathogen detection methods is increasingly important, and CRISPR-Cas system can be optimized for this purpose. CRISPR-Cas12a is a single RNA-guided endonuclease system with the potential for nucleic acid detection. There is a broad diversity among Cas12a nucleases with robust detection capability. Herein, we characterised three Cas12a orthologs (ObCas12a, MbCas12a, and ScCas12a), including cis- and transcleavage activities, the identification of PAM, single-base resolution ability, and the application for nucleic acid detection. These Cas12a orthologs displayed robust cis- and trans-cleavage activities, and performed well in terms of specificity and sensitivity for nucleic acid detection. Furthermore, they have subtle differences in single-base resolution and recognised PAM sites in vitro. Therefore, these Cas12a nucleases are candidate proteins for CRISPR-based diagnostic methods. Addition of these enzymes to the nucleic acid detection toolbox will further expand the utility of this powerful technology.
引用
收藏
页数:7
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