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CRISPR/Cas13a Trans-Cleavage-Triggered Catalytic Hairpin Assembly Assay for Specific and Ultrasensitive SARS-CoV-2 RNA Detection.
Yang, Yixia; Yi, Wenfu; Gong, Feng; Tan, Zhiyou; Yang, Yeling; Shan, Xiaoyun; Xie, Conghua; Ji, Xinghu; Zheng, Zhenhua; He, Zhike.
  • Yang Y; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
  • Yi W; State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, China.
  • Gong F; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
  • Tan Z; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
  • Yang Y; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
  • Shan X; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
  • Xie C; Department of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, and Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
  • Ji X; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
  • Zheng Z; State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, China.
  • He Z; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
Anal Chem ; 95(2): 1343-1349, 2023 01 17.
Article in English | MEDLINE | ID: covidwho-2185430
ABSTRACT
New coronavirus (SARS-CoV-2), which has caused the coronavirus disease 2019 (COVID-19) pandemic, has brought about a huge burden on global healthcare systems. Rapid and early detection is important to prevent the spread of the pandemic. Here, an assay based on CRISPR/Cas13a and catalytic hairpin assembly (CHA), termed as Cas-CHA, was developed for ultrasensitive and specific detection of SARS-CoV-2 RNA. Upon specific recognition of the target, the CRISPR/Cas13a collaterally cleaved a well-designed hairpin reporter and triggered the CHA reaction. Under optimized conditions, the assay detected the SARS-CoV-2 RNA with a wide range of 100 aM to 100 nM and realized a low detection limit of 84 aM. At the same time, the whole detecting process could be completed within 35 min. More importantly, the assay was able to distinguish SARS-CoV-2 RNA from common human coronaviruses and analyze in saliva samples. By the flexible design of crRNA, the assay was expanded to detect other viruses. The clinical sample analysis verified that the proposed assay held a great potential for practical testing.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Anal Chem Year: 2023 Document Type: Article Affiliation country: Acs.analchem.2c04306

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Anal Chem Year: 2023 Document Type: Article Affiliation country: Acs.analchem.2c04306