Electrical biosensing system utilizing ion-producing enzymes conjugated with aptamers for the sensing of severe acute respiratory syndrome coronavirus 2

Viral outbreaks, which include the ongoing coronavirus disease 2019 (COVID-19) pandemic provoked by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are a major global crisis that enormously threaten human health and social activities worldwide. Consequently, the rapid and repeated trea...

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Veröffentlicht in:Sensing and Bio-Sensing Research 2023-02, Vol.39, p.100549-100549, Article 100549
Hauptverfasser: Nukazuka, Akira, Asai, Satomi, Hayakawa, Kei, Nakagawa, Kazuhisa, Kanazashi, Mana, Kakizoe, Hidefumi, Hayashi, Kyoko, Kawahara, Toshio, Sawada, Kazuaki, Kuno, Hitoshi, Kano, Kazuhiko
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Sprache:eng
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Zusammenfassung:Viral outbreaks, which include the ongoing coronavirus disease 2019 (COVID-19) pandemic provoked by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are a major global crisis that enormously threaten human health and social activities worldwide. Consequently, the rapid and repeated treatment and isolation of these viruses to control their spread are crucial to address the COVID-19 pandemic and future epidemics of novel emerging viruses. The application of cost-efficient, rapid, and easy-to-operate detection devices with miniaturized footprints as a substitute for the conventional optic-based polymerase chain reaction (PCR) and immunoassay tests is critical. In this context, semiconductor-based electrical biosensors are attractive sensing platforms for signal readout. Therefore, this study aimed to examine the electrical sensing of patient-derived SARS-CoV-2 samples by harnessing the activity of DNA aptamers directed against spike proteins on viral surfaces. We obtained rapid and sensitive virus detection beyond the Debye length limitation by exploiting aptamers coupled with alkaline phosphatases, which catalytically generate free hydrogen ions which can readily be measured on pH meters or ion-sensitive field-effect transistors. Furthermore, we demonstrated the detection of the viruses of approximately 100 copies/μL in 10 min, surpassing the capability of typical immunochromatographic assays. Therefore, our newly developed technology has great potential for point-of-care testing not only for SARS-CoV-2, but also for other types of pathogens and biomolecules. •Traditional detection methods depend on the measurement of optical signals.•The proposed technique employed a DNA aptamer as the analyte recognition moiety.•The aptamers were conjugated with alkaline phosphatase.•The enzymes produce dispersing H+ ions to be measured on electrical devices.•Fast and sensitive detection of SARS-CoV-2 was achieved.
ISSN:2214-1804
2214-1804
DOI:10.1016/j.sbsr.2023.100549