Journal
ANALYTICAL LETTERS
Volume 47, Issue 3, Pages 478-491Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/00032719.2013.841179
Keywords
Adenosine triphosphate; Amplification detection; Aptamer; Enzyme-free; Strand displacement reaction
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Funding
- University of Science & Technology of China
- City University of Hong Kong
- National Natural Science Foundation of China [51073146, 21074122, 51103143, 51173175]
- Fundamental Research Funds for the Central Universities [WK2060200005]
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A strand displacement reaction-based system was developed for the determination of adenosine triphosphate (ATP). It involved an entropy-driven catalytic cycle that directly employed the ATP aptamer as the catalyst. Introduction of ATP into the system induced the catalyst to form the G-quadruplex conformation and inhibited its catalytic activity. All intermediates in the catalytic cycle processes were identified by polyacrylamide gel electrophoresis analysis. When the oligonucleotides were labeled with a carboxyfluorescein fluorophore and a 4-([4-(dimethylamino)phenyl]azo)benzoic acid quencher, this strand displacement reaction-based catalytic system exhibited a switch-on response for ATP. Conditions for detecting ATP, such as the toehold length, concentrations of the catalyst and magnesium ion, and incubation temperature, were optimized to obtain a detection limit of 50nM and a linear response up to 1400nM of ATP. This target inhibited catalytic cycle provides an enzyme-free biosensing strategy and has potential application in aptamer-based biosensing.
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