CRISPR/Cas Systems towards Next-Generation Biosensing

被引:700
作者
Li, Yi [1 ,2 ]
Li, Shiyuan [3 ]
Wang, Jin [4 ]
Liu, Guozhen [1 ,2 ,5 ]
机构
[1] Univ New South Wales, Fac Engn, ARC Ctr Excellence Nanoscale Biophoton, Grad Sch Biomed Engn, Sydney, NSW 2052, Australia
[2] Univ New South Wales, Australian Ctr NanoMed, Sydney, NSW 2052, Australia
[3] Shanghai Tolo Biotechnol Co Ltd, Shanghai 200233, Peoples R China
[4] Shanghai Normal Univ, Coll Life & Environm Sci, Shanghai 200234, Peoples R China
[5] Cent China Normal Univ, Coll Chem, Int Joint Res Ctr Intelligent Biosensor Technol &, Wuhan 430079, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
NUCLEIC-ACID DETECTION; ISOTHERMAL AMPLIFICATION; DIAGNOSTICS; CLASSIFICATION; EVOLUTION; ENDONUCLEASE; DIVERSITY; SEQUENCES; PLATFORM; POINT;
D O I
10.1016/j.tibtech.2018.12.005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Beyond its remarkable genome editing ability, the CRISPR/Cas9 effector has also been utilized in biosensing applications. The recent discovery of the collateral RNA cleavage activity of the Cas13a effector has sparked even greater interest in developing novel biosensing technologies for nucleic acid detection and promised significant advances in CRISPR diagnostics. Now, along with the discovery of Cas12 collateral cleavage activities on single-stranded DNA (ssDNA), several CRISPR/Cas systems have been established for detecting various targets, including bacteria, viruses, cancer mutations, and others. Based on key Cas effectors, we provide a detailed classification of CRISPR/Cas biosensing systems and propose their future utility. As the field continues to mature, CRISPR/Cas systems have the potential to become promising candidates for next-generation diagnostic biosensing platforms.
引用
收藏
页码:730 / 743
页数:14
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