DNA Sensor Integrated CRISPR-Cas9 and a Four-Electrode Probe
This paper presents an electrochemical DNA sensor integrating CRISPR -Cas9 target recognition, gold nanoparticle signal amplification, and a glassy carbon microelectrode array in a four-electrode anodic stripping voltammetry system. The use of microfluidics and a dedicated oxidation electrode enhances gold nanoparticle signal capture and mass transfer efficiency. Applied to lateral flow assay samples, the sensor achieved a detection limit of <tex xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">$5\times 10^{7} \ \text{copies}/\mu \mathrm{L}$</tex>, an improvement of two orders of magnitude compared to visual LFA intepretation, enabling more accurate detection of SARS CoV2 nucleic acid amplified by loop-mediated isothermal amplification. This platform significantly advances nucleic acid diagnostics by offering high sensitivity, quantification capability, and compatibility for point-of-collection testing.
Authors
- Tianhong Cui (ORCID: https://orcid.org/0000-0002-7427-2274)
- Mark J. Osborn (ORCID: https://orcid.org/0000-0003-1790-0841)
- Amber McElroy (ORCID: https://orcid.org/0000-0002-4169-0015)
- Peng Zhou (ORCID: https://orcid.org/0009-0003-0477-1566)
- Yingming Xu (ORCID: https://orcid.org/0009-0001-4613-1079)
Institutions
- University of Minnesota (US)
- University of Minnesota System (US)
Publication Details
- Published
- 2025-06-29
- DOI
- https://doi.org/10.1109/transducers61432.2025.11111229
- Citations
- 1
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- National Science Foundation