DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kyeonghye Guk | - |
dc.contributor.author | Soyeon Yi | - |
dc.contributor.author | Hyeran Kim | - |
dc.contributor.author | Yoonji Bae | - |
dc.contributor.author | D Yong | - |
dc.contributor.author | S Kim | - |
dc.contributor.author | Kyu-Sun Lee | - |
dc.contributor.author | Eun Kyung Lim | - |
dc.contributor.author | Taejoon Kang | - |
dc.contributor.author | Juyeon Jung | - |
dc.date.accessioned | 2022-10-31T16:32:38Z | - |
dc.date.available | 2022-10-31T16:32:38Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/30521 | - |
dc.description.abstract | Clustered 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.publisher | Elsevier | - |
dc.title | Hybrid CRISPR/Cas protein for one-pot detection of DNA and RNA | - |
dc.title.alternative | Hybrid CRISPR/Cas protein for one-pot detection of DNA and RNA | - |
dc.type | Article | - |
dc.citation.title | Biosensors & Bioelectronics | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 114819 | - |
dc.citation.startPage | 114819 | - |
dc.citation.volume | 219 | - |
dc.contributor.affiliatedAuthor | Kyeonghye Guk | - |
dc.contributor.affiliatedAuthor | Soyeon Yi | - |
dc.contributor.affiliatedAuthor | Hyeran Kim | - |
dc.contributor.affiliatedAuthor | Yoonji Bae | - |
dc.contributor.affiliatedAuthor | Kyu-Sun Lee | - |
dc.contributor.affiliatedAuthor | Eun Kyung Lim | - |
dc.contributor.affiliatedAuthor | Taejoon Kang | - |
dc.contributor.affiliatedAuthor | Juyeon Jung | - |
dc.contributor.alternativeName | 국경혜 | - |
dc.contributor.alternativeName | 이소연 | - |
dc.contributor.alternativeName | 김혜란 | - |
dc.contributor.alternativeName | 배윤지 | - |
dc.contributor.alternativeName | 용동은 | - |
dc.contributor.alternativeName | 김선주 | - |
dc.contributor.alternativeName | 이규선 | - |
dc.contributor.alternativeName | 임은경 | - |
dc.contributor.alternativeName | 강태준 | - |
dc.contributor.alternativeName | 정주연 | - |
dc.identifier.bibliographicCitation | Biosensors & Bioelectronics, vol. 219, pp. 114819-114819 | - |
dc.identifier.doi | 10.1016/j.bios.2022.114819 | - |
dc.subject.keyword | CRISPR/Cas | - |
dc.subject.keyword | DNA | - |
dc.subject.keyword | RNA | - |
dc.subject.keyword | Fusion protein | - |
dc.subject.keyword | Severe acute respiratory syndrome coronavirus 2 | - |
dc.subject.local | CRISPR-Cas | - |
dc.subject.local | crispr-cas | - |
dc.subject.local | CRISPR/Cas | - |
dc.subject.local | crispr/cas | - |
dc.subject.local | CRISPR/cas | - |
dc.subject.local | crispr cas | - |
dc.subject.local | DNA | - |
dc.subject.local | RNA | - |
dc.subject.local | Fusion protein | - |
dc.subject.local | fusion protein | - |
dc.subject.local | severe acute respiratory syndrome coronavirus 2 | - |
dc.subject.local | Severe acute respiratory syndrome coronavirus 2 | - |
dc.description.journalClass | Y | - |
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