Label-Free and Universal CRISPR/Cas12a-Based Detection Platform for Nucleic Acid Biomarkers

CRISPR/Cas12a has been widely used in molecular diagnostics due to its excellent trans-cleavage activity. However, conventional reporters, such as F/Q-labeled single-stranded DNA (ssDNA) reporters, enzyme-labeled reporters, and spherical nucleic acid reporters, require complex modification or labeling processes. In this study, we have developed a rapid, universal, and label-free CRISPR/Cas12a-based biomarker detection platform via designing a G-quadruplex (G4) containing a hairpin structure as the reporter. The hairpin loop design of hairpin G4 improves the cleavage efficiency of Cas12a and the signal strength of the G4 binding ligand. Meanwhile, the incorporation of a G4 binding dye (protoporphyrin IX) eliminates the need for complex modifications. The CRISPR-hairpin G4 detection platform is capable of detecting ssDNA, double-stranded DNA, genetic RNAs, and miRNAs. Moreover, this platform achieves label-free detection in clinical samples, demonstrating its practical applicability and efficiency.

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Publication Details

Journal
ACS Sensors
Published
2024-09-16
DOI
https://doi.org/10.1021/acssensors.4c01233
Citations
22
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
5.14

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article

Label-Free and Universal CRISPR/Cas12a-Based Detection Platform for Nucleic Acid Biomarkers

Rujian Zhao, Yao Xiao, Yidan Tang, Bingling Li et al.
22 citations
ACS Sensors
CRISPR and Genetic Engineering
5.14
article

Label-Free and Universal CRISPR/Cas12a-Based Detection Platform for Nucleic Acid Biomarkers

Rujian Zhao, Yao Xiao, Yidan Tang, Bingling Li, Baiyang Lu
article en
22 citations

Abstract

CRISPR/Cas12a has been widely used in molecular diagnostics due to its excellent trans-cleavage activity. However, conventional reporters, such as F/Q-labeled single-stranded DNA (ssDNA) reporters, enzyme-labeled reporters, and spherical nucleic acid reporters, require complex modification or labeling processes. In this study, we have developed a rapid, universal, and label-free CRISPR/Cas12a-based biomarker detection platform via designing a G-quadruplex (G4) containing a hairpin structure as the reporter. The hairpin loop design of hairpin G4 improves the cleavage efficiency of Cas12a and the signal strength of the G4 binding ligand. Meanwhile, the incorporation of a G4 binding dye (protoporphyrin IX) eliminates the need for complex modifications. The CRISPR-hairpin G4 detection platform is capable of detecting ssDNA, double-stranded DNA, genetic RNAs, and miRNAs. Moreover, this platform achieves label-free detection in clinical samples, demonstrating its practical applicability and efficiency.

ACS SensorsVol. 9(9)
University of Science and Technology of China (CN), Changchun Institute of Applied Chemistry (CN)
People's Government of Jilin Province
Openalex Percentile: Top 4%
CRISPR and Genetic Engineering
5.14
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Label-Free and Universal CRISPR/Cas12a-Based Detection Platform for Nucleic Acid Biomarkers — Rujian Zhao, Yao Xiao, et al. · ACS Sensors (2024) | TGRS Research Map | TGRS