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Abstract
A low limit of detection down to 2.1 aM is achieved for target miRNA using an enhanced CRISPR/Cas12a system.
- The assembly of multiple CRISPR/Cas12a units via hybridization chain reaction (HCR) enhances detection sensitivity.
- Improved cleavage efficiency is observed with the HCR/Cas12a system compared to a single Cas12a unit.
- A tetrahedral DNA nanostructure on the electrode surface facilitates excellent reactivity and accessibility for cleavage.
- The method demonstrates high specificity, storage stability, and accuracy for miRNA sensing in biological samples.
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