Based ATP-gating mechanism for detection of alkaline phosphatase in single-glass micropipettes functionalized by three-dimensional DNA network

• Published in: Mikrochimica acta (1966) 2024-06, Vol.191 (6), p.341-341, Article 341
• Main Authors: Zheng, Juanjuan, Zhang, Jinzheng, Xu, Shiwei, Feng, Yueyue, Huang, Liying, Wang, Guofeng, Liu, Nannan
• Format: Article
• Language: English
• Subjects: Adenosine triphosphate; Adenosine Triphosphate - analysis; Adenosine Triphosphate - chemistry; Adenosine Triphosphate - metabolism; Alkaline phosphatase; Alkaline Phosphatase - chemistry; Alkaline Phosphatase - metabolism; Analytical Chemistry; Ascorbic acid; Ascorbic Acid - analogs & derivatives; Ascorbic Acid - chemistry; Biological activity; Biomolecules; Biosensing Techniques - methods; Cascade chemical reactions; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; DNA - chemistry; Gating systems; Glass - chemistry; Hydroxyl radicals; Limit of Detection; Microengineering; Nanochemistry; Nanotechnology; Original Paper; Phosphatase; Terephthalic acid
• ISSN: 0026-3672; 1436-5073
• DOI: 10.1007/s00604-024-06400-6

The construction of gating system in artificial channels is a cutting-edge research direction in understanding biological process and application sensing. Here, by mimicking the gating system, we report a device that easily synthesized single-glass micropipettes functionalized by three-dimensional (3D) DNA network, which triggers the gating mechanism for the detection of biomolecules. Based on this strategy, the gating mechanism shows that single-glass micropipette assembled 3D DNA network is in the “OFF” state, and after collapsing in the presence of ATP, they are in the “ON” state, at which point they exhibit asymmetric response times. In the “ON” process of the gating mechanism, the ascorbic acid phosphate (AAP) can be encapsulated by a 3D DNA network and released in the presence of adenosine triphosphate (ATP), which initiates a catalyzed cascade reaction under the influence of alkaline phosphatase (ALP). Ultimately, the detection of ALP can be responded to form the fluorescence signal generated by terephthalic acid that has captured hydroxyl radicals, which has a detection range of 0–250 mU/mL and a limit of detection of 50 mU/mL. This work provides a brand-new way and application direction for research of gating mechanism. Graphical Abstract