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Electrochemical Impedance-Based Biosensors for the Label-Free Detection of the Nucleocapsid Protein from SARS-CoV-2

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dc.contributor.authorCho, Hana-
dc.contributor.authorShim, Suhyun-
dc.contributor.authorCho, Won Woo-
dc.contributor.authorCho, Sungbo-
dc.contributor.authorBaek, Hanseung-
dc.contributor.authorLee, Sang-Myung-
dc.contributor.authorShin, Dong-Sik-
dc.date.accessioned2023-11-08T09:44:02Z-
dc.date.available2023-11-08T09:44:02Z-
dc.date.issued2022-06-
dc.identifier.issn2379-3694-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/152728-
dc.description.abstractDiagnosis of coronavirus disease (COVID-19) is important because of the emergence and global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Real-time polymerase chain reaction (PCR) is widely used to diagnose COVID-19, but it is time-consuming and requires sending samples to test centers. Thus, the need to detect antigens for rapid on-site diagnosis rather than PCR is increasing. We quantified the nucleocapsid (N) protein in SARS-CoV-2 using an electro-immunosorbent assay (El-ISA) and a multichannel impedance analyzer with a 96-interdigitated microelectrode sensor (ToAD). The El-ISA measures impedance signals from residual detection antibodies after sandwich assays and thus offers highly specific, label-free detection of the N protein with low cross-reactivity. The ToAD sensor enables the real-time electrochemical detection of multiple samples in conventional 96-well plates. The limit of detection for the N protein was 0.1 ng/mL with a detection range up to 10 ng/mL. This system did not detect signals for the S protein. While this study focused on detecting the N protein in SARS-CoV-2, our system can also be widely applicable to detecting various biomolecules involved in antigen-antibody interactions.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleElectrochemical Impedance-Based Biosensors for the Label-Free Detection of the Nucleocapsid Protein from SARS-CoV-2-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acssensors.2c00317-
dc.identifier.scopusid2-s2.0-85132128957-
dc.identifier.wosid000818560300001-
dc.identifier.bibliographicCitationACS SENSORS, v.7, no.6, pp 1676 - 1684-
dc.citation.titleACS SENSORS-
dc.citation.volume7-
dc.citation.number6-
dc.citation.startPage1676-
dc.citation.endPage1684-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.subject.keywordPlusFLOW IMMUNO ASSAY-
dc.subject.keywordPlusFLUORESCENCE-
dc.subject.keywordPlusPCR-
dc.subject.keywordAuthorelectrochemical sensor-
dc.subject.keywordAuthornucleocapsid protein-
dc.subject.keywordAuthorSARS-CoV-2-
dc.subject.keywordAuthorimpedance-
dc.subject.keywordAuthorlabel-free detection-
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