Journal
ANALYTICAL CHEMISTRY
Volume 94, Issue 9, Pages 4119-4125Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c00294
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Funding
- National Natural Science Foundation of China [21475031, 21605034]
- Science and Technology Research Project of Higher Education of Hebei Province [ZD2021008]
- Science Fund for Creative Research Groups of Nature Science Foundation of Hebei Province [B2021201038]
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This study successfully combines the CRISPR-Cas12a system with the ligase chain reaction (LCR), achieving homogeneous, ultrasensitive, and visual detection of microRNA targets. By designing specific LCR probes and guide RNA, the LCR reaction is initiated and ultrasensitive detection is achieved through the secondary signal amplification mechanism of the Cas12a system. Moreover, microRNA can be visually detected by naked eyes and accurately quantified through image analysis using a cationic conjugated polymer.
The ligase chain reaction (LCR), as a classic nucleic acid amplification technique, is popular in the detection of DNA and RNA due to its simplicity, powerfulness, and high specificity. However, homogeneous and ultrasensitive LCR detection is still quite challenging. Herein, we integrate the LCR with a CRISPR-Cas12a system to greatly promote the application of the LCR in a homogeneous fashion. By employing microRNA as the model target, we design LCR probes with specific protospacer adjacent motif sequences and the guide RNA. Then, the LCR is initiated by target microRNA, and the LCR products specifically bind to the guide RNA to activate the Cas12a system, triggering secondary signal amplification to achieve ultrasensitive detection of microRNA without separation steps. Moreover, by virtue of a cationic conjugated polymer, microRNA can not only be visually detected by naked eyes but also be accurately quantified based on RGB ratio analysis of images with no need of sophisticated instruments. The method can quantify microRNA up to 4 orders of magnitude, and the determination limit is 0.4 aM, which is better than those of other reported studies using CRISPR-Cas12a and can be compared with that of the reverse-transcription polymerase chain reaction. This study demonstrates that the CRISPR-Cas12a system can greatly expand the application of the LCR for the homogeneous, ultrasensitive, and visual detection of microRNA, showing great potential in efficient nucleic acid detection and in vitro diagnosis.
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