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用于超灵敏核酸检测的单管巢式PCR与CRISPR-Cas12a联用技术

One-Tube Nested PCR Coupled with CRISPR-Cas12a for Ultrasensitive Nucleic Acid Testing.

作者信息

He Yugan, Peng Yadan, Tong Yigang

机构信息

Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, PR China.

College of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, PR China.

出版信息

ACS Omega. 2024 Sep 13;9(38):39616-39625. doi: 10.1021/acsomega.4c03911. eCollection 2024 Sep 24.

Abstract

Nucleic acid testing with high sensitivity and specificity is of great importance for accurate disease diagnostics. Here, we developed an in situ one-tube nucleic acid testing assay. In this assay, the target nucleic acid is captured using magnetic silica beads, avoiding an elution step, followed directly by the polymerase chain reaction (PCR) and clustered regularly interspaced short palindromic repeats (CRISPR)-Cas12a detection. This assay achieved visual readout and a sensitivity of 120 copies/mL for detecting SARS-CoV-2. More importantly, the assay demonstrated over 95% sensitivity and 100% specificity compared to the gold standard real-time quantitative PCR (RT-qPCR) test by using 75 SARS-CoV-2 clinical samples. By integrating nested PCR and Cas12a, this all-in-one nucleic acid testing approach enables ultrasensitive, highly specific, and cost-effective diagnosis at community clinics and township hospitals.

摘要

具有高灵敏度和特异性的核酸检测对于准确的疾病诊断至关重要。在此,我们开发了一种原位单管核酸检测方法。在该方法中,使用磁性硅胶珠捕获目标核酸,避免了洗脱步骤,然后直接进行聚合酶链反应(PCR)和规律成簇间隔短回文重复序列(CRISPR)-Cas12a检测。该方法实现了可视化读数,检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的灵敏度为120拷贝/毫升。更重要的是,通过使用75份SARS-CoV-2临床样本,与金标准实时定量PCR(RT-qPCR)检测相比,该方法显示出超过95%的灵敏度和100%的特异性。通过整合巢式PCR和Cas12a,这种一体化核酸检测方法能够在社区诊所和乡镇医院实现超灵敏、高特异性且经济高效的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a9/11425923/6f4c4ba28da2/ao4c03911_0001.jpg

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