用滚环扩增技术探索miRNA的反式切割活性。

Q2 Agricultural and Biological Sciences
生物设计研究(英文) Pub Date : 2023-03-27 eCollection Date: 2023-01-01 DOI:10.34133/bdr.0010
Chenqi Niu, Juewen Liu, Xinhui Xing, Chong Zhang
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引用次数: 0

摘要

微小RNA(miRNA)是一类内源性短非编码RNA。它们调节对生物过程至关重要的基因表达和功能。有必要开发一种有效的检测方法来确定这些对癌症诊断有价值的生物标志物。在本文中,我们提出了一种通用而快速的方法,通过将CRISPR-Cas12a和滚圈扩增(RCA)与预循环探针相结合来灵敏和定量地检测miRNA。最终,miRNA-21的检测可以在70分钟内完成,具有高特异性的检测极限为8.1pM。反应时间从超过5小时减少到70分钟,几乎减少了4小时,这使得检测更加有效。该设计提高了基于CRISPR-Cas和RCA的传感策略的效率,并在基于实验室的检测和护理点测试中显示出巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA.

Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA.

Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA.

Exploring the Trans-Cleavage Activity with Rolling Circle Amplification for Fast Detection of miRNA.

MicroRNAs (miRNAs) are a class of endogenous short noncoding RNA. They regulate gene expression and function, essential to biological processes. It is necessary to develop an efficient detection method to determine these valuable biomarkers for the diagnosis of cancers. In this paper, we proposed a general and rapid method for sensitive and quantitative detection of miRNA by combining CRISPR-Cas12a and rolling circle amplification (RCA) with the precircularized probe. Eventually, the detection of miRNA-21 could be completed in 70 min with a limit of detection of 8.1 pM with high specificity. The reaction time was reduced by almost 4 h from more than 5 h to 70 min, which makes detection more efficient. This design improves the efficiency of CRISPR-Cas and RCA-based sensing strategy and shows great potential in lab-based detection and point-of-care test.

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来源期刊
CiteScore
3.90
自引率
0.00%
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