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一种基于无PAM重组酶聚合酶扩增和CRISPR/Cas12a的一步法检测SARS-CoV-2 N基因的检测方法。

A one-pot assay based on PAM-free recombinase polymerase amplification and CRISPR/Cas12a for rapid detection of SARS-CoV-2 N gene.

作者信息

Yang Yixia, Ji Xinghu, Zhou Fuxiang, He Zhike

机构信息

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, China.

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, China.

出版信息

Talanta. 2026 Jan 1;296:128448. doi: 10.1016/j.talanta.2025.128448. Epub 2025 Jun 9.

Abstract

SARS-CoV-2 is a pathogenic virus, which exhibits high contagiousness. Therefore, a rapid and sensitive SARS-CoV-2 detection strategy is imperative. Herein, a one-pot assay by the combination of protospacer adjacent motif (PAM)-free recombinase polymerase amplification with CRISPR/Cas12a for detecting SARS-CoV-2 N gene was reported. To avoid the constraint of the PAM site for double-stranded DNA (dsDNA) in CRISPR/Cas12a system, we designed two individual crRNAs to hybridize with two different regions of the target sequence. The presence of N gene DNA was able to initiate the amplification of RPA, exposing the recognition site of crRNA and activating the Cas12a. Whereafter, the Cas12a activation resulted in the digestion of nontarget DNA reporters to induce significant fluorescence signal. The assay completed the detection of N gene DNA within 30 min. And a high sensitivity of 100 aM was obtained because of RPA amplification and Cas12a trans cleavage activity. Meanwhile, the proposed assay showed excellent specificity due to the site-specific recognition ability of CRISPR/Cas12a. More importantly, analysis of spiked samples verified the excellent practical application of the proposed method. Thus, the assay earned promising potential in molecular diagnostics.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是一种致病性病毒,具有高度传染性。因此,一种快速灵敏的SARS-CoV-2检测策略势在必行。在此,报道了一种通过无原间隔序列邻近基序(PAM)的重组酶聚合酶扩增与CRISPR/Cas12a相结合用于检测SARS-CoV-2 N基因的一锅法检测。为避免CRISPR/Cas12a系统中双链DNA(dsDNA)的PAM位点限制,我们设计了两个单独的crRNA与靶序列的两个不同区域杂交。N基因DNA的存在能够启动重组酶聚合酶扩增(RPA),暴露crRNA的识别位点并激活Cas12a。此后,Cas12a的激活导致非靶标DNA报告分子的消化,从而诱导显著的荧光信号。该检测在30分钟内完成了N基因DNA的检测。由于RPA扩增和Cas12a反式切割活性,获得了100 aM的高灵敏度。同时,由于CRISPR/Cas12a的位点特异性识别能力,所提出的检测方法显示出优异的特异性。更重要的是,对加标样品的分析验证了所提出方法的出色实际应用。因此,该检测方法在分子诊断中具有广阔的应用前景。

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