School of Pharmacy, Jiangsu University, Zhenjiang, 212013, PR China.
College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha, 410081, PR China.
Biosens Bioelectron. 2022 Nov 15;216:114683. doi: 10.1016/j.bios.2022.114683. Epub 2022 Sep 6.
Developing highly accurate and simple approaches to rapidly identify and isolate SARS-CoV-2 infected patients is important for the control of the COVID-19 pandemic. We, herein, reported the performance of a Cas12a-assisted RTF-EXPAR strategy for the identification of SARS-CoV-2 RNA. This assay combined the advantages of RTF-EXPAR with CRISPR-Cas12a can detect SARS-CoV-2 within 40 min, requiring only isothermal control. Particularly, the simultaneous use of EXPAR amplification and CRISPR improved the detection sensitivity, thereby realizing ultrasensitive SARS-CoV-2 RNA detection with a detection limit of 3.77 aM (∼2 copies/μL) in an end-point fluorescence read-out fashion, and at 4.81 aM (∼3 copies/μL) level via a smartphone-assisted analysis system (RGB analysis). Moreover, Cas12a increases the specificity by intrinsic sequence-specific template recognition. Overall, this method is fast, sensitive, and accurate, needing minimal equipment, which holds great promise to meet the requirements of point-of-care molecular detection of SARS-CoV-2.
开发高度准确和简单的方法来快速识别和隔离 SARS-CoV-2 感染患者对于控制 COVID-19 大流行非常重要。在此,我们报告了 Cas12a 辅助的 RTF-EXPAR 策略用于鉴定 SARS-CoV-2 RNA 的性能。该测定法将 RTF-EXPAR 与 CRISPR-Cas12a 的优势相结合,能够在 40 分钟内检测到 SARS-CoV-2,仅需等温控制。特别是,EXPAR 扩增和 CRISPR 的同时使用提高了检测灵敏度,从而实现了超灵敏的 SARS-CoV-2 RNA 检测,在终点荧光读取方式下的检测限为 3.77 aM(约 2 拷贝/μL),通过智能手机辅助分析系统(RGB 分析)为 4.81 aM(约 3 拷贝/μL)。此外,Cas12a 通过内在的序列特异性模板识别提高了特异性。总的来说,该方法快速、灵敏、准确,所需设备最少,有望满足 SARS-CoV-2 即时护理分子检测的要求。