Target Extension‐Activated DNA Walker on Nanoparticles for Digital Counting‐Based Analysis of MicroRNA
Main observation and conclusion MicroRNAs (miRNAs), especially exosomal miRNAs, are promising noninvasive biomarkers in early‐stage cancer diagnosis and disease treatment monitoring. However, their precise and sensitive quantification remains challenging due to their small size and low abundance. He...
Saved in:
Published in | Chinese journal of chemistry Vol. 39; no. 6; pp. 1471 - 1476 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY‐VCH Verlag GmbH & Co. KGaA
01.06.2021
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Main observation and conclusion
MicroRNAs (miRNAs), especially exosomal miRNAs, are promising noninvasive biomarkers in early‐stage cancer diagnosis and disease treatment monitoring. However, their precise and sensitive quantification remains challenging due to their small size and low abundance. Herein, we have developed a nanoparticle‐confined DNA walker strategy for the specific detection of miRNA. In the existence of the target miRNA, the on‐particle DNA walking reaction will be initiated, providing a fluorescence‐positive nanoparticle. Otherwise, the nanoparticle would be fluorescence‐negative. Utilizing the total internal reflection fluorescent microscope (TIRFM) to digitally count the fluorescence‐positive nanoparticles, the proposed method possesses a detection limit of 0.2 pmol/L miRNA and can accurately distinguish the single‐base mismatched target. This design combines the merits of the DNA walker for signal amplification and the TIRFM for highly sensitive detection, paving a new way for the digital counting‐based analysis of exosomal miRNAs.
A new DNA walking mechanism is developed for the digital counting‐based analysis of miRNA. |
---|---|
Bibliography: | † In Situ Target Biomolecule Analysis in Confined Nanospace. Dedicated to the Special Issue of |
ISSN: | 1001-604X 1614-7065 |
DOI: | 10.1002/cjoc.202000692 |