反式激活crRNA
清脆的
核酸
化学
DNA
病毒
分子诊断学
生物
材料科学
分子生物学
计算生物学
纳米技术
病毒学
基因组编辑
基因
生物化学
生物信息学
作者
Huahua Yue,Bowen Shu,Tian Tian,Erhu Xiong,Mengqi Huang,Debin Zhu,Jian Sun,Qing Liu,Shichan Wang,Yirong Li,Xiaoming Zhou
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-05-26
卷期号:21 (11): 4643-4653
被引量:163
标识
DOI:10.1021/acs.nanolett.1c00715
摘要
DNA quantification is important for biomedical research, but the routinely used techniques rely on nucleic acid amplification which have inherent issues like cross-contamination risk and quantification bias. Here, we report a CRISPR-Cas12a-based molecular diagnostic technique for amplification-free and absolute quantification of DNA at the single-molecule level. To achieve this, we first screened out the optimal reaction parameters for high-efficient Cas12a assay, yielding over 50-fold improvement in sensitivity compared with the reported Cas12a assays. We further leveraged the microdroplet-enabled confinement effect to perform an ultralocalized droplet Cas12a assay, obtaining excellent specificity and single-molecule sensitivity. Moreover, we demonstrated its versatility and quantification capability by direct counting of diverse virus's DNAs (African swine fever virus, Epstein–Barr virus, and Hepatitis B virus) from clinical serum samples with a wide range of viral titers. Given the flexible programmability of crRNA, we envision this amplification-free technique as a versatile and quantitative platform for molecular diagnosis.
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