清脆的
核酸
核酸检测
重组酶聚合酶扩增
反式激活crRNA
计算生物学
聚合酶链反应
基因组编辑
Cas9
环介导等温扩增
生物
DNA
遗传学
基因
作者
Jian Zhou,Zhuo Li,Joshua Seun Olajide,Gang Wang
出处
期刊:Heliyon
[Elsevier]
日期:2024-02-01
卷期号:10 (4): e26179-e26179
被引量:12
标识
DOI:10.1016/j.heliyon.2024.e26179
摘要
CRISPR/Cas systems have become integral parts of nucleic acid detection apparatus and biosensors. Various CRISPR/Cas systems such as CRISPR/Cas9, CRISPR/Cas12, CRISPR/Cas13, CRISPR/Cas14 and CRISPR/Cas3 utilize different mechanisms to detect or differentiate biological activities and nucleotide sequences. Usually, CRISPR/Cas-based nucleic acid detection systems are combined with polymerase chain reaction, loop-mediated isothermal amplification, recombinase polymerase amplification and transcriptional technologies for effective diagnostics. Premised on these, many CRISPR/Cas-based nucleic acid biosensors have been developed to detect nucleic acids of viral and bacterial pathogens in clinical samples, as well as other applications in life sciences including biosecurity, food safety and environmental assessment. Additionally, CRISPR/Cas-based nucleic acid detection systems have showed better specificity compared with other molecular diagnostic methods. In this review, we give an overview of various CRISPR/Cas-based nucleic acid detection methods and highlight some advances in their development and components. We also discourse some operational challenges as well as advantages and disadvantages of various systems. Finally, important considerations are offered for the improvement of CRISPR/Cas-based nucleic acid testing.
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