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Cited 30 time in webofscience Cited 29 time in scopus
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Hybrid CRISPR/Cas protein for one-pot detection of DNA and RNA

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dc.contributor.authorGuk, Kyeonghye-
dc.contributor.authorYi, Soyeon-
dc.contributor.authorKim, Hyeran-
dc.contributor.authorBae, Yoonji-
dc.contributor.authorYong, Dongeun-
dc.contributor.authorKim, Sunjoo-
dc.contributor.authorLee, Kyu-Sun-
dc.contributor.authorLim, Eun-Kyung-
dc.contributor.authorKang, Taejoon-
dc.contributor.authorJung, Juyeon-
dc.date.accessioned2024-12-02T22:00:57Z-
dc.date.available2024-12-02T22:00:57Z-
dc.date.issued2023-01-
dc.identifier.issn0956-5663-
dc.identifier.issn1873-4235-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/72309-
dc.description.abstractClustered regularly interspaced short palindromic repeats (CRISPR)-based diagnostics have emerged as next -generation molecular diagnostics. In CRISPR-based diagnostics, Cas12 and Cas13 proteins have been widely employed to detect DNA and RNA, respectively. Herein, we developed a novel hybrid Cas protein capable of detecting universal nucleic acids (DNA and RNA). The CRISPR/hybrid Cas system simultaneously recognizes both DNA and RNA, enabling the dual detection of pathogenic viruses in a single tube. Using wild-type (WT) and N501Y mutant severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as detection models, we suc-cessfully detected both virus strains with a detection limit of 10 viral copies per reaction without cross-reactivity. Furthermore, it is demonstrated the detection of WT SARS-CoV-2 and N501Y mutant variants in clinical samples by using the CRISPR/hybrid Cas system. The hybrid Cas protein is expected to be utilized in a molecular diagnostic method for infectious diseases, tissue and liquid biopsies, and other nucleic acid biomarkers.-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER ADVANCED TECHNOLOGY-
dc.titleHybrid CRISPR/Cas protein for one-pot detection of DNA and RNA-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.bios.2022.114819-
dc.identifier.scopusid2-s2.0-85140480652-
dc.identifier.wosid000884797500001-
dc.identifier.bibliographicCitationBIOSENSORS & BIOELECTRONICS, v.219-
dc.citation.titleBIOSENSORS & BIOELECTRONICS-
dc.citation.volume219-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.subject.keywordPlusASSAY-
dc.subject.keywordPlusSARS-COV-2-
dc.subject.keywordAuthorCRISPR-
dc.subject.keywordAuthorCas-
dc.subject.keywordAuthorDNA-
dc.subject.keywordAuthorRNA-
dc.subject.keywordAuthorFusion protein-
dc.subject.keywordAuthorSevere acute respiratory syndrome coronavirus-
dc.subject.keywordAuthor2-
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