化学
CpG站点
甲基化
表观遗传学
DNA甲基化
计算生物学
灵敏度(控制系统)
检出限
生物系统
分辨率(逻辑)
癌症
DNA
结直肠癌
生物传感器
癌症检测
极限(数学)
生物物理学
癌症研究
癌症生物标志物
分子生物学
作者
Songkuan Zhuang,Ganfeng Deng,Zhenghua Xie,Li Zhang,Yizhen Liu
标识
DOI:10.1021/acs.analchem.6c05211
摘要
Abstract Accurate single-CpG methylation analysis in dense regions is critical for cancer diagnostics but challenged by adjacent CpG interference. Here, we developed EPICATCH, an interference-tolerant ratiometric Cas13a biosensor to overcome this limitation. Exploiting LbuCas13a′s asymmetric mismatch sensitivity, we established a dual-zone recognition framework. Positioning the target CpG in the strictly sensitive 5′-zone guarantees single-base resolution, while placing adjacent CpGs in the tolerant 3′-zone masks epigenetic noise, achieving a 7-bp spatial resolution for the tested MYO1G construct. Integrated with recombinase polymerase amplification, ssDNA generation, and a dual-channel ratiometric readout, EPICATCH eliminates sample concentration biases, achieving a 100 aM limit of detection. Applying EPICATCH to quantify MYO1G methylation in clinical plasma cfDNA from colorectal cancer patients yielded a clinical sensitivity of 80.0% and specificity of 84.6%. This dual-zone recognition system provides a robust strategy for precise single-CpG analysis and cancer screening.
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