化学
清脆的
串联
N6-甲基腺苷
分辨率(逻辑)
基础(拓扑)
核糖核酸
计算生物学
色谱法
分子生物学
DNA
生物化学
甲基转移酶
基因
甲基化
数学分析
材料科学
数学
人工智能
生物
计算机科学
复合材料
作者
Kunyu Shi,Yong Zhang,Yiran Tao,Yuxi Wang,Jinliang Yang,Ruijie Deng,Hao Yang
标识
DOI:10.1021/acs.analchem.4c06782
摘要
N6-Methyladenosine (m6A) ranks among the most prevalent modifications in RNA, which serves as a biomarker for diseases, such as lung cancer. Herein, we developed a CRISPR/Cas13a-Csm6 tandem assay (termed CRISPRm6A assay) allowing for preamplification-free, sensitive, and rapid detection of RNA m6A modifications. The coupling of Cas13a-Csm6 tandem with MazF endoribonuclease enables the assay to identify m6A RNA with single-base resolution. Compared to the CRISPRm6A assay using Cas13a alone, the tandem CRISPRm6A assay yielded an improved sensitivity for RNA detection by ∼22 times, thus enabling preamplification-free detection of RNA m6A. Particularly, the proposed assay enabled quantification of m6A abundance down to 0.5% at the picomole level in lncRNA MALAT1 and demonstrated a 100% correlation in diagnosing nonsmall cell lung cancer. In summary, the CRISPRm6A assay supports two key applications in biological samples: (1) precise determination of m6A sites and (2) quantitative measurement of m6A fractions. Therefore, the CRISPR tandem method presents a promising tool for RNA epigenetics-based diagnostics.
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