4.2 Article

Construction of a Sensing Platform Based on DNA-Encoded Magnetic Beads and Copper Nanoclusters for Viral Gene Analysis with Target Recycling Amplification

Journal

ACS APPLIED BIO MATERIALS
Volume 4, Issue 7, Pages 5669-5677

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsabm.1c00460

Keywords

fluorescence; magnetic separation; CuNCs; target recycling amplification; label-free

Funding

  1. National Natural Science Foundation of China [21775052, 21575048]
  2. Science and Technology Development Project of Jilin province, China [20180414013GH]

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The study successfully designed a sensing system that combined target DNA recycling amplification, magnetic separation, and fluorescent copper nanoclusters (CuNCs) technologies for sensitive and specific detection of viral DNA. By combining magnetic beads and fluorescent CuNCs, a universal, label-free, and reusable platform for viral DNA detection was achieved.
The rapid and accurate monitoring of viral genes plays an important role in the area of disease diagnosis, biomedical research, and food safety. Herein, we successfully designed a sensing system that combined the technologies of target DNA recycling amplification, magnetic separation, and in situ formation of fluorescent copper nanoclusters (CuNCs) for viral DNA analysis. In the presence of target viral DNA (tDNA), a large quantity of output DNA (oDNA) was produced from hairpin DNA (hDNA) through an exonuclease III-assisted target recycling amplification strategy. Magnetic beads (MBs) labeled with capture DNA (cDNA) were hybridized with oDNA, and the partially complementary oDNA served as a bridge that could link AT-rich dsDNA on the surface of MBs, which led to a decrease of AT-rich dsDNA in solution after magnetic separation. On account of the lack of AT-rich dsDNA as a template in solution, in situ formation of fluorescent CuNCs was blocked, which resulted in a decrease in the fluorescence intensity at 590 nm. Therefore, taking advantage of one-step magnetic separation and in situ formation of CuNCs, the target viral DNA was sensitively and specifically detected in a linear range from 5 pM to 5 nM with a detection limit of 1 pM. The MB-based platform was not only reusable but also achieved magnetic separation, which could eliminate interferences in complex samples. The assay combining the MB-based probe with fluorescent CuNCs provided a universal, label-free, and reusable platform for viral DNA detection.

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