Tian Zimu, Yan He, Zeng Yong
medRxiv. 2023 Apr 29:2023.04.28.23289279. doi: 10.1101/2023.04.28.23289279.
Public healthcare demands effective and pragmatic diagnostic tools to address the escalating challenges in infection management in resource-limited areas. Recent advance in CRISPR-based biosensing promises the development of next-generation tools for disease diagnostics, including point-of-care (POC) testing for infectious diseases. Currently prevailing strategy of developing CRISPR assays exploits only the non-specific trans-cleavage function of a CRISPR-Cas12a/Cas13a system for detection and combines it with an additional pre-amplification reaction to enhance the sensitivity. In contrast to this single-function strategy, here we present a new approach that collaboratively integrates the dual functions of CRISPR-Cas12a: sequence-specific binding and trans-cleavage activity. With this approach, we developed a POC nucleic acid assay termed Solid-Phase Extraction and Enhanced Detection assay Integrated by CRISPR-Cas12a (SPEEDi-CRISPR) that negates the need for preamplification but significantly improves the detection of limit (LOD) from the pM to fM level. Specifically, using Cas12a-coated magnetic beads, this assay combines efficient solid-phase extraction and enrichment of DNA targets enabled by the sequence-specific affinity of CRISPR-Cas12a with the fluorogenic detection by the activated Cas12a on beads. Our proof-of-concept study demonstrated that the SPEEDi-CRISPR assay affords an improved detection sensitivity for human papillomavirus (HPV)-18 with a LOD of 2.3 fM and excellent specificity to discriminate HPV-18 from HPV-16, Parvovirus B19, and scramble HPV-18. Furthermore, this robust assay was readily coupled with a portable smartphone-based fluorescence detector and a lateral flow assay for quantitative detection and visualized readout, respectively. Overall, these results should suggest that our dual-function strategy could pave a new way for developing the next-generation CRISPR diagnostics and that the SPEEDi-CRISPR assay provides a potentially useful tool for point-of-care testing.
公共卫生保健需要有效且实用的诊断工具,以应对资源有限地区感染管理方面不断升级的挑战。基于CRISPR的生物传感技术的最新进展有望开发出用于疾病诊断的下一代工具,包括传染病的即时检测(POC)。目前开发CRISPR检测的主流策略仅利用CRISPR-Cas12a/Cas13a系统的非特异性反式切割功能进行检测,并将其与额外的预扩增反应相结合以提高灵敏度。与这种单功能策略不同,我们在此提出一种新方法,该方法协同整合了CRISPR-Cas12a的双重功能:序列特异性结合和反式切割活性。通过这种方法,我们开发了一种即时核酸检测方法,称为CRISPR-Cas12a整合的固相萃取和增强检测法(SPEEDi-CRISPR),该方法无需预扩增,但能将检测限(LOD)从皮摩尔水平显著提高到飞摩尔水平。具体而言,该检测方法使用包被Cas12a的磁珠,将CRISPR-Cas12a的序列特异性亲和力实现的高效固相萃取和DNA靶标的富集与磁珠上活化的Cas12a的荧光检测相结合。我们的概念验证研究表明,SPEEDi-CRISPR检测方法对人乳头瘤病毒(HPV)-18具有更高的检测灵敏度,检测限为2.3飞摩尔,并且在区分HPV-18与HPV-16、细小病毒B19和乱序HPV-18方面具有出色的特异性。此外,这种强大的检测方法很容易分别与基于便携式智能手机的荧光检测器和侧向流动检测法相结合,用于定量检测和可视化读数。总体而言,这些结果表明我们的双功能策略可为开发下一代CRISPR诊断方法开辟一条新途径,并且SPEEDi-CRISPR检测方法为即时检测提供了一种潜在有用的工具。