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DNAzyme-mediated fluorescence signal variation of DNA-Ag nanoclusters and construction of an aptasensor for ATP.

Authors :
Cai S
Li M
Hu X
Gui S
Li M
Zhang Y
Wang X
Zhou N
Source :
Analytical methods : advancing methods and applications [Anal Methods] 2024 Nov 21; Vol. 16 (45), pp. 7676-7682. Date of Electronic Publication: 2024 Nov 21.
Publication Year :
2024

Abstract

DNA-templated silver nanoclusters (DNA-AgNCs) are novel nanomaterials with unique fluorescence characteristics. DNAzyme is a functional oligonucleotide that can catalyze the disruption of nucleic acid substrates. In this research, the effect of DNAzyme digestion on the fluorescence property of DNA-AgNCs was explored for the first time. A significant reduction in the fluorescence intensity of DNA-AgNCs after cleavage by DNAzyme was discovered. Further research found that the DNAzyme-catalyzed cleavage reduced the stability of DNA-AgNCs and led to their aggregation, accounting for a decline in fluorescence intensity up to 84%. Inspired by the above finding, a fluorescent aptasensor that integrates the benefits of DNA-AgNCs, exonuclease III (Exo III)-assisted signal amplification and DNAzyme was developed for sensitive detection of adenosine triphosphate (ATP). Under optimal conditions, the linear range was from 25 μM to 1000 μM and the detection limit was estimated to be 4.46 μM. Furthermore, this fluorescent aptasensor was effectively employed to quantify ATP levels in human serum samples, demonstrating its practicality in detecting ATP in biological matrices. The elucidation of DNAzyme-based fluorescence characteristic variation of DNA-AgNCs may provide insights into the interactions between DNAzyme and nanomaterials and has great prospects in the construction of fluorescent biosensors.

Details

Language :
English
ISSN :
1759-9679
Volume :
16
Issue :
45
Database :
MEDLINE
Journal :
Analytical methods : advancing methods and applications
Publication Type :
Academic Journal
Accession number :
39403815
Full Text :
https://doi.org/10.1039/d4ay01608d