Hybrid CRISPR/Cas protein for one-pot detection of DNA and RNA

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dc.contributor.authorKyeonghye Guk-
dc.contributor.authorSoyeon Yi-
dc.contributor.authorHyeran Kim-
dc.contributor.authorYoonji Bae-
dc.contributor.authorD Yong-
dc.contributor.authorS Kim-
dc.contributor.authorKyu-Sun Lee-
dc.contributor.authorEun Kyung Lim-
dc.contributor.authorTaejoon Kang-
dc.contributor.authorJuyeon Jung-
dc.date.accessioned2022-10-31T16:32:38Z-
dc.date.available2022-10-31T16:32:38Z-
dc.date.issued2022-
dc.identifier.issn0956-5663-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/30521-
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 successfully 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.publisherElsevier-
dc.titleHybrid CRISPR/Cas protein for one-pot detection of DNA and RNA-
dc.title.alternativeHybrid CRISPR/Cas protein for one-pot detection of DNA and RNA-
dc.typeArticle-
dc.citation.titleBiosensors & Bioelectronics-
dc.citation.number0-
dc.citation.endPage114819-
dc.citation.startPage114819-
dc.citation.volume219-
dc.contributor.affiliatedAuthorKyeonghye Guk-
dc.contributor.affiliatedAuthorSoyeon Yi-
dc.contributor.affiliatedAuthorHyeran Kim-
dc.contributor.affiliatedAuthorYoonji Bae-
dc.contributor.affiliatedAuthorKyu-Sun Lee-
dc.contributor.affiliatedAuthorEun Kyung Lim-
dc.contributor.affiliatedAuthorTaejoon Kang-
dc.contributor.affiliatedAuthorJuyeon Jung-
dc.contributor.alternativeName국경혜-
dc.contributor.alternativeName이소연-
dc.contributor.alternativeName김혜란-
dc.contributor.alternativeName배윤지-
dc.contributor.alternativeName용동은-
dc.contributor.alternativeName김선주-
dc.contributor.alternativeName이규선-
dc.contributor.alternativeName임은경-
dc.contributor.alternativeName강태준-
dc.contributor.alternativeName정주연-
dc.identifier.bibliographicCitationBiosensors & Bioelectronics, vol. 219, pp. 114819-114819-
dc.identifier.doi10.1016/j.bios.2022.114819-
dc.subject.keywordCRISPR/Cas-
dc.subject.keywordDNA-
dc.subject.keywordRNA-
dc.subject.keywordFusion protein-
dc.subject.keywordSevere acute respiratory syndrome coronavirus 2-
dc.subject.localCRISPR-Cas-
dc.subject.localcrispr-cas-
dc.subject.localCRISPR/Cas-
dc.subject.localcrispr/cas-
dc.subject.localCRISPR/cas-
dc.subject.localcrispr cas-
dc.subject.localDNA-
dc.subject.localRNA-
dc.subject.localFusion protein-
dc.subject.localfusion protein-
dc.subject.localsevere acute respiratory syndrome coronavirus 2-
dc.subject.localSevere acute respiratory syndrome coronavirus 2-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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