Rapid and sensitive detection of circulating tumor DNA <i>via</i> a CRISPR/Cas12a-based catalytic hairpin assembly

Cancer is one of the major diseases that endanger the human health. Circulating tumor DNA (ctDNA) is an ideal biomarker for the real-time monitoring of cancer. In the present work, a rapid and sensitive assay coupled with CRISPR/Cas12a and CHA (Cas12a-CHA) was constructed for the detection of ctDNA. We designed and prepared a trigger, which was the substrate of Cas12a. On the addition of ctDNA, crRNA-guided ctDNA activated the <i>trans</i>-endonuclease activity of Cas12a. After being activated, Cas12a exhibited a high <i>trans</i>-cleavage activity on the trigger, which resulted in a decrease in fluorescence. Owing to this design, the Cas12a-CHA assay enabled the sensitive detection of ctDNA with a linear range of 10 fM to 50 pM. Furthermore, a limit-of-detection of 5.8 fM was achieved within 40 min. Besides, the proposed assay had an excellent base mismatch recognition ability and worked well in human serum samples. Conclusively, this detection platform holds significant potential for application in early cancer diagnosis.

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Publication Details

Journal
Analytical Methods
Published
2025-11-22
DOI
https://doi.org/10.1039/d5ay01624j
Citations
1
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
0.81
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article

Rapid and sensitive detection of circulating tumor DNA via a CRISPR/Cas12a-based catalytic hairpin assembly

Lingzi Yao, Feng Gong, Ying Li, Songbai Tian et al.
1 citations
Analytical Methods
Advanced biosensing and bioanalysis techniques
0.81
article

Rapid and sensitive detection of circulating tumor DNA via a CRISPR/Cas12a-based catalytic hairpin assembly

Lingzi Yao, Feng Gong, Ying Li, Songbai Tian, Yixia Yang, Yujie Zhao
article en
1 citations

Abstract

Cancer is one of the major diseases that endanger the human health. Circulating tumor DNA (ctDNA) is an ideal biomarker for the real-time monitoring of cancer. In the present work, a rapid and sensitive assay coupled with CRISPR/Cas12a and CHA (Cas12a-CHA) was constructed for the detection of ctDNA. We designed and prepared a trigger, which was the substrate of Cas12a. On the addition of ctDNA, crRNA-guided ctDNA activated the <i>trans</i>-endonuclease activity of Cas12a. After being activated, Cas12a exhibited a high <i>trans</i>-cleavage activity on the trigger, which resulted in a decrease in fluorescence. Owing to this design, the Cas12a-CHA assay enabled the sensitive detection of ctDNA with a linear range of 10 fM to 50 pM. Furthermore, a limit-of-detection of 5.8 fM was achieved within 40 min. Besides, the proposed assay had an excellent base mismatch recognition ability and worked well in human serum samples. Conclusively, this detection platform holds significant potential for application in early cancer diagnosis.

Analytical MethodsVol. 18(1)
North Sichuan Medical University (CN), Hubei University of Medicine (CN), Guangxi University (CN), Sun Yat-sen University (CN), Guangxi Medical University (CN), The Seventh Affiliated Hospital of Sun Yat-sen University (CN)
Openalex Percentile: Top 21%
Advanced biosensing and bioanalysis techniques
0.81
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Rapid and sensitive detection of circulating tumor DNA <i>via</i> a CRISPR/Cas12a-based catalytic hairpin assembly — Lingzi Yao, Feng Gong, et al. · Analytical Methods (2025) | TGRS Research Map | TGRS