Recent progress in aptamer and CRISPR-Cas12a based systems for non-nucleic target detection
文献类型: 外文期刊
作者: Yang, Ruiqi 1 ; Zhao, Liping 1 ; Wang, Xinjie 1 ; Kong, Weijun 2 ; Luan, Yunxia 1 ;
作者机构: 1.Inst Qual Stand & Testing Technol BAAFS, Agr Prod Qual & Safety Risk Assessment Lab, Dept Agr, Beijing 100097, Peoples R China
2.Chengdu Univ Tradit Chinese Med, Coll Pharm, Chengdu, Peoples R China
3.Chengdu Univ Tradit Chinese Med, Coll Pharm, Chengdu 611137, Peoples R China
关键词: Aptamer; biosensor; CRISPR-Cas12a; non-nucleic acid target
期刊名称:CRITICAL REVIEWS IN ANALYTICAL CHEMISTRY ( 影响因子:5.0; 五年影响因子:5.3 )
ISSN: 1040-8347
年卷期: 2023 年
页码:
收录情况: SCI
摘要: Efficient and sensitive detection of targets is one of the motivations for constant development and innovation of various biosensors. CRISPR-Cas12a, a new generation of gene editing tools, has shown excellent application potential in biosensor design and construction. By combining with the specific recognition element-aptamer, a single-stranded oligonucleotide obtained by systematic evolution of ligands by exponential enrichment (SELEX) in vitro screening, CRISPR-Cas12a also shows superior performance non-nucleic acid targets detection, such as small molecules, proteins, virus and pathogenic bacteria. However, aptamer and CRISPR-Cas12a (CRISPR-Cas12a/Apt) still face some problems in non-nucleic acid target detection, such as single signal response mode and narrow linear range. The development of diverse CRISPR-Cas12a/Apt biosensors is necessary to meet the needs of various detection environments. In this review, the working principle of CRISPR-Cas12a/Apt was introduced and recent progress in CRISPR-Cas12a/Apt in the application of non-nucleic acid target detection was summarized. Moreover, the requirements of critical parameters such as crRNA sequence, activator sequence, and reaction system in the design of CRISPR-Cas12a/Apt biosensors were discussed, which could provide the reference for the design of efficient and sensitive novel non-nucleic acid target biosensors. In addition, the challenges and prospects of CRISPR-Cas12a/Apt-based biosensor were further presented.
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