清脆的
放大器
核酸扩增试验
重组酶聚合酶扩增
微流控
核酸
反式激活crRNA
化学
计算生物学
Cas9
聚合酶链反应
DNA
纳米技术
病毒学
环介导等温扩增
生物
基因
材料科学
生物化学
沙眼衣原体
作者
Yong Chen,Nan Zong,Feidi Ye,Yixin Mei,Jiuxin Qu,Xingyu Jiang
标识
DOI:10.1021/acs.analchem.2c00638
摘要
The clustered regularly interspaced short palindromic repeats (CRISPR)-based nucleic acid detection can be combined with recombinase-aided amplification (RAA) to enable rapid, accurate, and early detection of SARS-CoV-2. Current CRISPR-based approaches to detecting viral nucleic acid typically require immense manual operations to transfer RPA amplicons for CRISPR detection or suffer from compromised sensitivity by mixing the competing RPA amplification and CRISPR detection. Here, we develop dual-CRISPR/Cas12a-assisted RT-RAA assay and a ″sample-to-answer″ centrifugal microfluidic platform that can automatically detect 1 copy/μL of the SARS-CoV-2 within 30 min. This chip separates the amplification (RAA) from detection (CRISPR), such that sensitivity is maximized and the time consumption is decreased by a factor of 3. For the 26 positive and 8 negative clinical SARS-CoV-2 samples, this automated centrifugal microfluidics achieved 100% accuracy compared to the gold-standard RT-PCR technique. This point-of-care test, with the advantages of being one-step, automated, rapid, and sensitive, will have a significant potential for clinical diagnosis and disease prevention.
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