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A pH-responsive bioassay for sensitive colorimetric detection of adenosine triphosphate based on switchable DNA aptamer and metal ion-urease interactions.
Zhu, Sha; Yang, Yiqi; Li, Menglu; Yang, Yi; Li, Chao; Yin, Yongmei.
Afiliación
  • Zhu S; Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, People's Republic of China.
  • Yang Y; Department of Oncology, The Affiliated Wuxi No.2 People's Hospital of Nanjing Medical University, Wuxi, 214000, People's Republic of China.
  • Li M; Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, People's Republic of China.
  • Yang Y; State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210093, People's Republic of China.
  • Li C; State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210093, People's Republic of China.
  • Yin Y; School of Food and Biological Engineering, Hefei University of Technology, Hefei, 230009, People's Republic of China. lchao@hfut.edu.cn.
Anal Bioanal Chem ; 413(6): 1533-1540, 2021 Mar.
Article en En | MEDLINE | ID: mdl-33462658
ABSTRACT
A facile and economic colorimetric strategy was designed for ATP detection by rationally using urease, a pH-responsive molecule, and a metal-mediated switchable DNA probe. By utilizing metal ions as a modulator of urease activity, the concentration of ATP is translated into pH change, which can be readily visualized by naked eye. An unmodified single-stranded DNA probe was designed, which consists of a target binding sequence and two flanked cytosine (C)-rich sequences. This C-rich single-stranded DNA can form a hairpin structure triggered by Ag+ ions via C-Ag+-C base mismatch. Upon introduction of ATP, Ag+-coordinated hairpin DNA structure will be broken and release the included Ag+, thus inhibiting the activity of urease. Conversely, urease can hydrolyze urea and raise pH value of the solution, resulting in the color change of the sensing solution. The proposed assay allows determination of ATP as low as 1.6 nM and shows a satisfactory result in human serum. Because of simple operation and low cost of this method, we believe it has a potential in point-of-care (POC) testing in resource-limited areas. Schematic illustration of pH-responsive colorimetric sensor for ATP detection based on switchable DNA aptamer and metal ion-urease interactions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Técnicas Biosensibles / Adenosina Trifosfato / Colorimetría / Aptámeros de Nucleótidos / Iones / Metales Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Anal Bioanal Chem Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Técnicas Biosensibles / Adenosina Trifosfato / Colorimetría / Aptámeros de Nucleótidos / Iones / Metales Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Anal Bioanal Chem Año: 2021 Tipo del documento: Article