Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Park, Sungwook | - |
dc.contributor.author | Kim, Hojun | - |
dc.contributor.author | Woo Kyoungmin | - |
dc.contributor.author | Kim, Jeong-Min | - |
dc.contributor.author | Jo, Hye-Jun | - |
dc.contributor.author | Jeong, Youngdo | - |
dc.contributor.author | Lee, Kwan Hyi | - |
dc.date.accessioned | 2024-01-19T13:01:31Z | - |
dc.date.available | 2024-01-19T13:01:31Z | - |
dc.date.created | 2022-04-03 | - |
dc.date.issued | 2022-01 | - |
dc.identifier.issn | 1530-6984 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/115841 | - |
dc.description.abstract | SARS-CoV-2 variants are of particular interest because they can potentially increase the transmissibility and virulence of COVID-19 or reduce the effectiveness of available vaccines. However, screening SARS-CoV-2 variants is a challenge because biosensors target viral components that can mutate. One promising strategy is to screen variants via angiotensin-converting enzyme 2 (ACE2), a virus receptor shared by all known SARS-CoV-2 variants. Here we designed a highly sensitive and portable COVID-19 screening biosensor based on the virus receptor. We chose a dualgate field-effect transistor to overcome the low sensitivity of virusreceptor-based biosensors. To optimize the biosensor, we introduced a synthetic virus that mimics the important features of SARS-CoV-2 (size, bilayer structure, and composition). The developed biosensor successfully detected SARS-CoV-2 in 20 min and showed sensitivity comparable to that of molecular diagnostic tests (similar to 165 copies/ mL). Our results indicate that a virus-receptor-based biosensor can be an effective strategy for screening infectious diseases to prevent pandemics. | - |
dc.language | English | - |
dc.publisher | American Chemical Society | - |
dc.title | SARS-CoV-2 Variant Screening Using a Virus-Receptor-Based Electrical Biosensor | - |
dc.type | Article | - |
dc.identifier.doi | 10.1021/acs.nanolett.1c03108 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | Nano Letters, v.22, no.1, pp.50 - 57 | - |
dc.citation.title | Nano Letters | - |
dc.citation.volume | 22 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 50 | - |
dc.citation.endPage | 57 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000737851900001 | - |
dc.identifier.scopusid | 2-s2.0-85122290424 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
dc.relation.journalWebOfScienceCategory | Physics, Applied | - |
dc.relation.journalWebOfScienceCategory | Physics, Condensed Matter | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.relation.journalResearchArea | Physics | - |
dc.type.docType | Article; Early Access | - |
dc.subject.keywordPlus | CORONAVIRUS | - |
dc.subject.keywordPlus | COVID-19 | - |
dc.subject.keywordPlus | SPIKE | - |
dc.subject.keywordPlus | DIAGNOSIS | - |
dc.subject.keywordPlus | SENSOR | - |
dc.subject.keywordAuthor | SARS-CoV-2 | - |
dc.subject.keywordAuthor | variant screening | - |
dc.subject.keywordAuthor | ACE2 | - |
dc.subject.keywordAuthor | virus receptor | - |
dc.subject.keywordAuthor | biosensor | - |
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