4.8 Article

Swing Arm Location-Controllable DNA Walker for Electrochemiluminescence Biosensing

Journal

ANALYTICAL CHEMISTRY
Volume 93, Issue 8, Pages 4051-4058

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c05051

Keywords

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Funding

  1. NNSF of China [22022408]
  2. Chongqing Talents Personnel Support Program [CQYC201905067]
  3. Fundamental Research Funds for the Central Universities [XDJK2019TJ002]

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A novel swing arm location-controllable DNA walker based on DNA tetrahedral nanostructures was developed for nucleic acid detection, demonstrating enhanced efficiency and potential in diagnostic analysis.
Here, we described a novel swing arm location-controllable DNA walker based on the DNA tetrahedral nanostructures (DTNs) for nucleic acid detection using the polycyclic aromatic hydrocarbon (PAH) microcrystals (TAPE-Pe MCs) consisting of the nonplanar molecular tetrakis(4-aminophenyl)ethene (TAPE) and planar molecular perylene (Pe) as electrochemiluminescence (ECL) luminophores. Specifically, the swing arm strands and track strands were fixed simultaneously on the DTNs to obtain the locationcontrollable DNA walker, which possessed an improved reaction efficiency compared to that of a fixed swing arm-based DNA walker due to the quantitative and orderly swing arm on the DTNs. On the other hand, the Pe microcrystals doped by TAPE molecules could decrease the pi-pi stacking of Pe molecules for the ECL efficiency enhancement, achieving a blue-shifted and intense ECL emission. Therefore, we defined this enhanced and blue-shifted ECL phenomenon as inhibition of conjugation-driven ECL (IC-ECL). To prove these principles, a location-controllable DNA walker-based ECL biosensor was developed with microRNA let-7a as target molecules. The ECL biosensor achieved a low detection limit of 4.92 fM within a wide linear range from 10 fM to 100 nM. This approach offers a new insight for ECL efficiency increase and location-controllable strategies with improved reaction efficiency, demonstrating potential in diagnostic analysis.

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