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

Author:

Niu Chenqi12,Liu Juewen2,Xing Xinhui13,Zhang Chong13

Affiliation:

1. MOE Key Laboratory for Industrial Biocatalysis, Institute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.

2. Department of Chemistry, Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Avenue West, Waterloo, ON N2L 3G1, Canada.

3. Center for Synthetic and Systems Biology, Tsinghua University, Beijing 100084, China.

Abstract

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.

Funder

National Key Research and Development Program of China

Joint Funds of the National Natural Science Foundation of China

National Natural Science Foundation of China

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Agricultural and Biological Sciences (miscellaneous),Biochemistry, Genetics and Molecular Biology (miscellaneous),Biotechnology

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