| Literature DB >> 33991961 |
Tao Li1, Rui Hu1, Jianbo Xia2, Zhichen Xu1, Dongjuan Chen2, Jinou Xi2, Bi-Feng Liu3, Jiang Zhu1, Ying Li4, Yunhuang Yang1, Maili Liu5.
Abstract
CRISPR-Cas12a (Cpf1) trans-cleaves ssDNA and this feature has been widely harnessed for nucleic acid detection. Herein, we introduce a new type of Cas12a reporter, G-triplex (G3), and a highly sensitive biosensor termed G-CRISPR. We proved that Cas12a trans-cleaves G3 structures in about 10 min and G3 can serve as an excellent reporter based on the cleavage-induced high-order structure disruption. G3 reporter improves the analytical sensitivity up to 20 folds, enabling the detection of unamplified and amplified DNA as low as 50 pmol and 0.1 amol (one copy/reaction), respectively. G-CRISPR has been utilized for the analysis of 27 PCR-amplified patient samples with HPV infection risk based on both fluorescence and lateral flow assays, resulting in 100% concordance between the two. In comparison with the clinical results, it achieved overall specificity and sensitivity of 100% and 94.7%, respectively. These results suggest that G-CRISPR can serve as a rapid, sensitive, and reliable biosensor, and could further expand the CRISPR toolbox in biomedical diagnostics.Entities:
Keywords: Biosensor; CRISPR-Cas12a; G-triplex; Nucleic acid detection; Trans-cleavage
Year: 2021 PMID: 33991961 DOI: 10.1016/j.bios.2021.113292
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618