An Enzyme-Triggered Au–Se Nanodevice for Precise Imaging of MicroRNA

In situ imaging of microRNA (miRNA) in tumor cells is vital for clinical diagnosis and pathological research. However, achieving high-precision imaging is always limited by undesirable background signals. Herein, we introduced a gold-selenium-based nanodevice (AuSeND) for high-fidelity imaging of miRNA via enzyme-triggered catalytic hairpin assembly (CHA). This system employs an enzyme-activatable CHA circuit, constructed by extending a short tail at the 3' end of hairpin H1 with an apurinic/apyrimidinic (AP) site. The CHA circuit components are connected to the surface of AuNPs via Au-Se bonds, forming a Au-Se nanodevice. It remains inactive in normal cells, while in tumor cells, the CHA circuit is activated by apurinic/apyrimidinic endonuclease 1 (APE1) in the cytoplasm, generating a fluorescence signal under miRNA stimulation for miRNA imaging. The developed AuSeND enables cancer cell-selective miRNA imaging and improves the signal-to-noise ratio by combining the high stability of the Au-Se bond with the specific regulation of the APE1 enzyme, offering strong potential for clinical diagnostic applications.

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Publication Details

Journal
Analytical Chemistry
Published
2025-04-15
DOI
https://doi.org/10.1021/acs.analchem.5c00395
Citations
4
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
3.22

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article

An Enzyme-Triggered Au–Se Nanodevice for Precise Imaging of MicroRNA

Peng Miao, Wei Pan, Yingbo Pan, Ruyue Wei et al.
4 citations
Analytical Chemistry
Advanced biosensing and bioanalysis techniques
3.22
article

An Enzyme-Triggered Au–Se Nanodevice for Precise Imaging of MicroRNA

Peng Miao, Wei Pan, Yingbo Pan, Ruyue Wei, Na Li, Shuqi Wang, Bo Tang
article en
4 citations

Abstract

In situ imaging of microRNA (miRNA) in tumor cells is vital for clinical diagnosis and pathological research. However, achieving high-precision imaging is always limited by undesirable background signals. Herein, we introduced a gold-selenium-based nanodevice (AuSeND) for high-fidelity imaging of miRNA via enzyme-triggered catalytic hairpin assembly (CHA). This system employs an enzyme-activatable CHA circuit, constructed by extending a short tail at the 3' end of hairpin H1 with an apurinic/apyrimidinic (AP) site. The CHA circuit components are connected to the surface of AuNPs via Au-Se bonds, forming a Au-Se nanodevice. It remains inactive in normal cells, while in tumor cells, the CHA circuit is activated by apurinic/apyrimidinic endonuclease 1 (APE1) in the cytoplasm, generating a fluorescence signal under miRNA stimulation for miRNA imaging. The developed AuSeND enables cancer cell-selective miRNA imaging and improves the signal-to-noise ratio by combining the high stability of the Au-Se bond with the specific regulation of the APE1 enzyme, offering strong potential for clinical diagnostic applications.

Analytical ChemistryVol. 97(16)
Chinese Academy of Sciences (CN), Shandong Normal University (CN), Suzhou Institute of Biomedical Engineering and Technology (CN), Ministry of Education (ME), Laoshan Laboratory
National Natural Science Foundation of China
Openalex Percentile: Top 9%
Advanced biosensing and bioanalysis techniques
3.22
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An Enzyme-Triggered Au–Se Nanodevice for Precise Imaging of MicroRNA — Peng Miao, Wei Pan, et al. · Analytical Chemistry (2025) | TGRS Research Map | TGRS