Wu Lina, Wang Xinjie, Wu Xiangchuan, Xu Shiqi, Liu Ming, Cao Xizhong, Tang Taishan, Huang Xingxu, Huang He
School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, Nanjing 210023, People's Republic of China.
Zhejiang Laboratory, Hangzhou 311100, People's Republic of China.
ACS Appl Mater Interfaces. 2022 Nov 16;14(45):50534-50542. doi: 10.1021/acsami.2c14497. Epub 2022 Oct 27.
The CRISPR-Cas system was developed into a molecular diagnostic tool with high sensitivity, low cost, and high specificity in recent years. Colorimetric assays based on nanozymes offer an attractive point-of-care testing method for their low cost of use and user-friendly operation. Here, a MnO nanozyme-mediated CRISPR-Cas12a system was instituted to detect SARS-CoV-2. MnO nanorods linked to magnetic beads via a single-stranded DNA (ssDNA) linker used as an oxidase-like nanozyme inducing the color change of 3,3',5,5'-tetramethylbenzidine, which can be distinguished by the naked eye. The detection buffer color will change when the Cas12a is activated by SARS-CoV-2 and indiscriminately cleave the linker ssDNA. The detection limit was 10 copies per microliter and showed no cross-reaction with other coronaviruses. The nanozyme-mediated CRISPR-Cas12a system shows high selectivity and facile operation, with great potential for molecular diagnosis in point-of-care testing applications.
近年来,CRISPR-Cas系统已发展成为一种具有高灵敏度、低成本和高特异性的分子诊断工具。基于纳米酶的比色测定法因其使用成本低且操作方便,提供了一种有吸引力的即时检测方法。在此,构建了一种MnO纳米酶介导的CRISPR-Cas12a系统来检测新型冠状病毒。通过单链DNA(ssDNA)接头与磁珠相连的MnO纳米棒用作类氧化酶纳米酶,可诱导3,3',5,5'-四甲基联苯胺发生颜色变化,肉眼即可区分。当Cas12a被新型冠状病毒激活并随机切割接头ssDNA时,检测缓冲液的颜色会发生变化。检测限为每微升10个拷贝,且与其他冠状病毒无交叉反应。纳米酶介导的CRISPR-Cas12a系统具有高选择性和操作简便的特点,在即时检测应用中的分子诊断方面具有巨大潜力。