4.7 Article

Element probe based CRISPR/Cas14 bioassay for non-nucleic-acid targets

期刊

CHEMICAL COMMUNICATIONS
卷 57, 期 80, 页码 10423-10426

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc03992j

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资金

  1. National Natural Science Foundation of China [22074098, 22074096]
  2. Recruitment Program of Global Experts of Sichuan Province [903]
  3. Fundamental Research Funds for the Central Universities

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A novel element probe based CRISPR/Cas14 detection platform was proposed in this study, allowing sensitive and quantitative detection of non-nucleic-acid targets such as trace aqueous ampicillin within 45 minutes at room temperature. The method showed excellent performance in anti-interference tests and complex matrix detection, with a low detection limit of 2.06 nM.
Herein, we propose an element probe based CRISPR/Cas14 detection platform and apply it to the detection of non-nucleic-acid targets. Combining metal isotope detection and CRISPR/Cas14 biosensing, the sensitive detection of non-nucleic-acid targets could be realized. We designed and optimized the element probe, which proved that Cas14 has a preference for longer lengths in element probe cleavage. Using this method, the quantitative detection of trace aqueous ampicillin can be achieved within 45 minutes at room temperature (25 degrees C). A detection limit as low as 2.06 nM is obtained with excellent performance in anti-interference tests and complex matrix detection.

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