Ma Peixiang, Meng Qingzhou, Sun Baoqing, Zhao Bing, Dang Lu, Zhong Mingtian, Liu Siyuan, Xu Hongtao, Mei Hong, Liu Jia, Chi Tian, Yang Guang, Liu Ming, Huang Xingxu, Wang Xinjie
Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Affiliated Cancer Hospital & Institute of Guangzhou Medical University 78 Hengzhigang Road Guangzhou 510095 China.
Adv Sci (Weinh). 2020 Sep 23;7(20):2001300. doi: 10.1002/advs.202001300. eCollection 2020 Oct.
Cas12a-based systems, which detect specific nucleic acids via collateral cleavage of reporter DNA, display huge potentials for rapid diagnosis of infectious diseases. Here, the Manganese-enhanced Cas12a (MeCas12a) system is described, where manganese is used to increase the detection sensitivity up to 13-fold, enabling the detection of target RNAs as low as five copies. MeCas12a is also highly specific, and is able to distinguish between single nucleotide polymorphisms (SNPs) differing by a single nucleotide. MeCas12a can detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in clinical samples and distinguish between SARS-CoV-2 and Middle East respiratory syndrome coronavirus (MERS-CoV) RNA in simulated samples, thus offering an attractive alternative to other methods for the diagnosis of infectious diseases including COVID-19 and MERS.
基于Cas12a的系统通过对报告DNA的旁切来检测特定核酸,在传染病的快速诊断方面显示出巨大潜力。在此,描述了锰增强型Cas12a(MeCas12a)系统,其中锰用于将检测灵敏度提高至13倍,能够检测低至五个拷贝的靶RNA。MeCas12a也具有高度特异性,能够区分相差单个核苷酸的单核苷酸多态性(SNP)。MeCas12a可以检测临床样本中的严重急性呼吸综合征冠状病毒2(SARS-CoV-2),并在模拟样本中区分SARS-CoV-2和中东呼吸综合征冠状病毒(MERS-CoV)RNA,从而为包括COVID-19和MERS在内的传染病诊断提供了一种有吸引力的替代其他方法的手段。