4.7 Article

A ratiometric electrochemical aptasensor for ultrasensitive determination of adenosine triphosphate via a triple-helix molecular switch

Journal

MICROCHIMICA ACTA
Volume 186, Issue 7, Pages -

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-019-3630-3

Keywords

Ratiometric strategy; Differential pulse voltammetry; Aptamer-target interaction; Triple-helix nucleic acid hybridization; Methylene blue; Ferrocene; Adenosine analogs; Structure variation

Funding

  1. National Natural Science Foundation of China [21864006, 21563006, 21763005]
  2. Natural Science Foundation of Guangxi Province [2017GXNSFDA198034, 2016GXNSFBA380118, 2017GXNSFFA198005]
  3. Guangxi Scientific and Technological Development Projects [AD17195081]
  4. China Scholarship Council Project [201708455047, liujinfa[2017]5086]
  5. Thousands of Young Teachers Training Program of Guangxi Province [guijiaoren[2018]18]
  6. High-Level-Innovation Team [guijiaoren[2017]38]
  7. Outstanding Scholar Project of Guangxi Higher Education Institutes
  8. BAGUI Scholar Program of Guangxi Province of China

Ask authors/readers for more resources

A ratiometric electrochemical aptamer-based assay is described for the ultrasensitive and highly specific determination of adenosine triphosphate (ATP). It is based on ATP aptamer-mediated triple-helix molecular switch (THMS). The method uses (a) a hairpin DNA (MB-DNA-SH) labeled with the redox probe Methylene Blue (MB) at the 3 end, and a thiol group at the 5 end, and (b) a single strand ATP aptamer modified with two ferrocenes at each end (Fc-DNA-Fc). The labeled probe of type MB-DNA-SH was self-assembled onto the surface of a gold electrode via gold-thiol binding. On exposure to Fc-DNA-Fc, it will hybridize with MB-DNA-SH to form a stable THMS structure on electrode surface. In the presence of ATP, it hybridizes with the loop portion of Fc-DNA-Fc, and this results in the unwinding of the THMS structure. Such variation caused the changes of the differential pulse voltammetry (DPV) peak currents of both MB (at around -0.25 V) and Fc (at around 0.39 V; both vs. Ag/AgCl). A significant enhancement is found for the ratio of the two DPV peaks. Under the optimum experimental conditions, this assay has a response that covers the 0.05 to 100 pM ATP concentration range, and the detection limit is 5.2 fM (for S/N = 3). The method is highly selective for ATP over its analogs.

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