Luwei Chai, Xinge Cui, Hongbing Liu, Yongkang Zhang, Yangwei Pan, Chenxi Li, Tao Le
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引用次数: 0
Abstract
The clustered regularly interspaced short palindromic repeats (CRISPR)/Cas systems, known for its high specificity and programmability, has demonstrated significant potential in single nucleotide polymorphisms (SNPs) detection and has been extensively applied in pathogen identification, genetic screening, and tumor mutation analysis. However, the relatively low turnover rates of cis- and trans-cleavage activities limit the specificity and sensitivity of CRISPR-based SNP detection systems. In response, various CRISPR/Cas-based SNP detection strategies have been developed to achieve ultrasensitive signal responses via diverse signal amplification techniques, thereby enhancing detection resolution. This review begins by summarizing the current status and challenges of CRISPR/Cas-based SNP detection technologies, then focuses on four representative strategies for enhancing CRISPR-SNP performance. Finally, we discuss future developments that may improve the efficiency of CRISPR-SNP detection systems.
期刊介绍:
TrAC publishes succinct and critical overviews of recent advancements in analytical chemistry, designed to assist analytical chemists and other users of analytical techniques. These reviews offer excellent, up-to-date, and timely coverage of various topics within analytical chemistry. Encompassing areas such as analytical instrumentation, biomedical analysis, biomolecular analysis, biosensors, chemical analysis, chemometrics, clinical chemistry, drug discovery, environmental analysis and monitoring, food analysis, forensic science, laboratory automation, materials science, metabolomics, pesticide-residue analysis, pharmaceutical analysis, proteomics, surface science, and water analysis and monitoring, these critical reviews provide comprehensive insights for practitioners in the field.