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April 24, 2026Analytical Chemistry2 citations

Amplified Assembly of a Multifunctional 3D DNA Nanomachine for Electrochemical and Colorimetric Dual-Mode Assays

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GFGuopei FangYLY. LiuWHWan Huang

Key Points

  • This research aims to develop a novel dual-mode biosensing method using a 3D DNA nanomachine to detect estrogen pollutants.
  • Constructed a multifunctional 3D DNA nanomachine utilizing aptamer recognition and catalytic hairpin assembly
  • Conducted electrochemical and colorimetric assays with detection ranges from 0.01 pg mL-1 to 10 ng mL-1
  • Utilized iron-based metal-organic frameworks (Fe-MOFs) to enhance signal amplification and assay reliability.
  • Achieved detection limits of 3.9 fg mL-1 (electrochemical) and 10.5 fg mL-1 (colorimetric)
  • Demonstrated excellent repeatability and reliability through cross-validation of both detection modes
  • Showed a wide linear detection range for both electrochemical and colorimetric assays.

Abstract

DNA nanomachines have been widely applied in biosensing; however, further enhancing their signal amplification capability and assay reliability remains a major challenge. Herein, a novel strategy was proposed to construct a multifunctional three-dimensional DNA nanomachine for the development of an electrochemical and colorimetric dual-mode biosensing method for detecting the estrogen pollutant 17β-estradiol. Aptamer recognition-triggered catalytic hairpin assembly, together with a cascade Nb.BbvCI-assisted DNA polymerization reaction, drove the amplified assembly of the DNA nanomachine composed of multiple triangular prism units. The abundant Mg2+-dependent DNAzymes formed on the nanomachine enabled its efficient walking on an iron-based metal-organic framework (Fe-MOF)-modified electrode, thereby generating an electrochemical signal. Meanwhile, numerous G-quadruplexes were formed accompanying the DNA nanomachine assembly, thereby enabling sensitive colorimetric signal readout through the excellent peroxidase-mimicking activity of the formed G-quadruplex/hemin DNAzymes, synergistically promoted by released Fe-MOFs. Consequently, the proposed method exhibited wide linear ranges of 0.01 pg mL-1 to 1 ng mL-1 (electrochemical) and 0.1 pg mL-1 to 10 ng mL-1 (colorimetric) with detection limits as low as 3.9 fg mL-1 and 10.5 fg mL-1, respectively. In addition, the method showed simple operation, excellent repeatability, and enhanced reliability through cross-validation between the dual detection modes. Therefore, this work provides a robust and sensitive approach for monitoring environmental estrogen pollutants.

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Cite This Study

Fang et al. (2026) studied this question.

synapsesocial.com/papers/69eb09ff553a5433e34b43a9https://doi.org/10.1021/acs.analchem.5c08259
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