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Updated: Jun 17, 2026

Probe-based Real-time PCR Approaches for Quantitative Measurement of microRNAs
Published on: April 14, 2015
Enzyme-assisted catalytic hairpin assembly based aggregation-induced emission assay for trace miRNA-196a in serum
Zihan Xu1, Yongda Lu2, Jieyu Yan3
1School of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230026, China.
None:
MicroRNA-196a (miRNA-196a) is a clinically significant biomarker for the early diagnosis of pancreatic cancer. However, its trace level in serum necessitates highly sensitive and robust detection methods. Combining the merits of the enzyme-free CHA DNA circuits and the nucleotide enzymes, an enzyme-assisted CHA (eaCHA) strategy is proposed and verified in an AIE biosensing platform targeting miRNA-196a to further boost amplification of CHA. The target (miRNA-196a) initiated an Nb·BbvCI assisted CHA, the products of which drove the assembly of two TPE-labeled probes (Probe 1 and Probe 2), resulting in a significant "turn on" of AIE signals. To further enhance sensitivity, exonuclease III was employed to assist the TS1 recycling from blunt-ended duplexes, enabling cascaded signal amplification. The biosensor exhibited a wide linear range from 1 pM to 50 nM with a detection limit of 120 fM. Generally, the assay demonstrated high selectivity, excellent reproducibility (RSD < 3%), and excellent performance in clinical sample assay, indicating its potential capability for early pancreatic cancer screening.

