A DNA octahedral amplifier for endogenous circRNA detection and bioimaging in living cells and its biomarker study

The discovery of reliable biomarkers is essential for early diagnosis, treatment, and prognosis assessment of diseases. Many research studies have shown that circRNA is a potential biomarker for diagnosis and prognosis of diseases. However, in situ monitoring circRNA in live cells is still a challen...

Full description

Saved in:
Bibliographic Details
Published in:Analyst (London) 2024-01, Vol.149 (3), p.87-814
Main Authors: Feng, Rong, Yu, Shengrong, Qian, Zhiling, Wang, Yiming, Xie, Gege, Li, Bingqian, Chen, Jingwen, Wu, Yong-Xiang, Tang, Keqi
Format: Article
Language:English
Subjects:
Amplifiers
Apexes
Biomarkers
Biosensing Techniques - methods
Carbocyanines
Cells (biology)
Diagnosis
DNA - genetics
Energy transfer
Health services
Limit of Detection
Medical imaging
MicroRNAs - genetics
Nuclease
Penetration resistance
Prognosis
RNA, Circular - genetics
Self-assembly
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The discovery of reliable biomarkers is essential for early diagnosis, treatment, and prognosis assessment of diseases. Many research studies have shown that circRNA is a potential biomarker for diagnosis and prognosis of diseases. However, in situ monitoring circRNA in live cells is still a challenge at present, which brings a major limitation to the development and verification of circRNA as a disease biomarker. In this study, a catalytic hairpin assembly (CHA) reaction-based DNA octahedral amplifier (DOA) was developed for fluorescence resonance energy transfer (FRET) detection and bioimaging of circRNA in living cells. The DOA was first produced by self-assembling a DNA octahedron with six customized single-stranded DNAs, and two hairpins H1 (Cy3) and H2 (Cy5) were then hybridized to four vertices of the DNA octahedron. Idiopathic pulmonary fibrosis (IPF)-related circHIPK3 was used as the target. Once the CHA reaction from H1 and H2 on DOA was activated by a sequence-specific back-splice junction (BSJ) of circHIPK3, a significant FRET signal can be obtained from Cy3 to Cy5. The circHIPK3 was subsequently released to cause the next CHA reaction. Because the DOA has the advantages of the spatial-confinement effect, resistance to nuclease degradation and easy penetration into cells, rapid and excellent signal amplification FRET detection and bioimaging of endogenous circHIPK3 can be achieved in various cells. This study provides a high-precision assay platform to explore the possibility of using circRNA as a biomarker, and it is valuable for circRNA-related early diagnosis and treatment of diseases. A DNA octahedral amplifier (DOA) nanoprobe was constructed as a fluorescence assay platform for in situ FRET detection and bioimaging of circRNA in living cells.
ISSN:0003-2654
1364-5528
DOI:10.1039/d3an01803b