State Key Laboratory of Magnetic Resonance and Atomic Molecular Physics, Wuhan National Laboratory for Optoelectronics, National Centre for Magnetic Resonance in Wuhan, Wuhan Institute of Physics and Mathematics, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences - Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, 430071, China; University of Chinese Academy of Sciences, Beijing, 10049, China.
Department of Laboratory Medicine, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430070, China.
Biosens Bioelectron. 2021 Sep 1;187:113292. doi: 10.1016/j.bios.2021.113292. Epub 2021 May 9.
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.
CRISPR-Cas12a (Cpf1) 可对单链 DNA 进行反式切割,这一特性已被广泛应用于核酸检测。在此,我们引入了一种新型的 Cas12a 报告分子 G-三链体 (G3),并构建了一种高灵敏度的生物传感器 G-CRISPR。我们证明 Cas12a 在约 10 分钟内即可切割 G3 结构,且 G3 因其切割引起的高级结构破坏,可作为优异的报告分子。G3 报告分子将分析灵敏度提高了 20 倍,可检测未经扩增和扩增的 DNA,其检测限分别低至 50 pmol 和 0.1 amol(每个反应/拷贝)。我们利用 G-CRISPR 对 27 例 HPV 感染风险的 PCR 扩增患者样本进行了分析,基于荧光和侧向流两种检测方法,其结果具有 100%的一致性。与临床结果相比,G-CRISPR 具有 100%的总体特异性和 94.7%的总体灵敏度。这些结果表明,G-CRISPR 可作为一种快速、灵敏、可靠的生物传感器,进一步扩展了 CRISPR 在生物医学诊断中的工具包。