State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200032, P. R. China.
Central Laboratory, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, P. R. China.
Angew Chem Int Ed Engl. 2023 Aug 7;62(32):e202305536. doi: 10.1002/anie.202305536. Epub 2023 Jun 27.
The trans-cleavage property of CRISPR-Cas12a system makes it an excellent tool for disease diagnosis. Nevertheless, most methods based on CRISPR-Cas system still require pre-amplification of the target to achieve the desired detection sensitivity. Here we generate Framework-Hotspot reporters (FHRs) with different local densities to investigate their effect on trans-cleavage activity of Cas12a. We find that the cleavage efficiency increases and the cleavage rate accelerates with increasing reporter density. We further construct a modular sensing platform with CRISPR-Cas12a-based target recognition and FHR-based signal transduction. Encouragingly, this modular platform enables sensitive (100 fM) and rapid (<15 min) detection of pathogen nucleic acids without pre-amplification, as well as detection of tumor protein markers in clinical samples. The design provides a facile strategy for enhanced trans cleavage of Cas12a, which accelerates and broadens its applications in biosensing.
CRISPR-Cas12a 系统的跨切割特性使其成为疾病诊断的优秀工具。然而,大多数基于 CRISPR-Cas 系统的方法仍需要对靶标进行预扩增,以达到所需的检测灵敏度。在这里,我们生成了具有不同局部密度的框架热点报告子(FHR),以研究它们对 Cas12a 的跨切割活性的影响。我们发现,随着报告子密度的增加,切割效率增加,切割速率加快。我们进一步构建了一个基于 CRISPR-Cas12a 的靶标识别和基于 FHR 的信号转导的模块化传感平台。令人鼓舞的是,这个模块化平台能够实现对病原体核酸的灵敏(100 fM)和快速(<15 min)检测,而无需预扩增,并且能够检测临床样本中的肿瘤蛋白标志物。该设计为增强 Cas12a 的跨切割提供了一种简便的策略,加速并拓宽了其在生物传感中的应用。