Quantitative detection of circular RNA and microRNA at point-of-care using droplet digital CRISPR/Cas13a platform

清脆的 小RNA 注意事项 核糖核酸 数字聚合酶链反应 计算生物学 点(几何) 计算机科学 生物 医学 数学 遗传学 病理 基因 聚合酶链反应 几何学
作者
Ke Wang,Haofan Yin,Shengli Li,Yunzhu Wan,Minmin Xiao,Xiaopeng Yuan,Zhenheng Huang,Yunxin Gao,Jianhua Zhou,Keying Guo,Jiasi Wang
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:267: 116825-116825 被引量:37
标识
DOI:10.1016/j.bios.2024.116825
摘要

Circular RNA (circRNA) and microRNA (miRNA) are both non-coding RNAs (ncRNAs) that serve as biomarkers for cancer diagnosis and prognosis. Quantitative detection of these ncRNAs is of particular importance to elucidate the functional mechanisms and evaluate their potential as biomarkers. However, the inherent structures of circRNA and miRNA are different from the mRNA, conventional qRT-PCR is unsuitable for the detection of these ncRNAs. Here, we propose a sensitive method for quantitative detection of circRNA and miRNA using polydisperse droplet digital CRISPR/Cas13a (PddCas13a). It can achieve limits of detection (LOD) as low as ∼10 aM without polymerase-based amplification. To efficiently detect the circRNA and miRNA in real samples, we use a chemically modified crRNA to enhance the stability of crRNA and improve the performance of Cas13a in complex environments containing contaminants. By integrating an extraction-free procedure with PddCas13a, we experimentally demonstrate the applicability of PddCas13a by testing clinical samples. Furthermore, we develop an automated and portable instrument for PddCas13a and verify its applicability for the detection of circRNA and miRNA from exosomes in point-of-care (POC) setting. This is the first report to detect the circRNA and miRNA simultaneously in POC setting. We envision this platform could promote the research of ncRNAs.
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