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Enhanced delivery of protein fused to cell penetrating peptides to mammalian cells

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dc.contributor.authorMoon, Jung-Il-
dc.contributor.authorHan, Min-Joon-
dc.contributor.authorYu, Shin-Hye-
dc.contributor.authorLee, Eun-Hye-
dc.contributor.authorKim, Sang-Mi-
dc.contributor.authorHan, Kyuboem-
dc.contributor.authorPark, Chang-Hwan-
dc.contributor.authorKim, Chun-Hyung-
dc.date.accessioned2022-07-09T18:06:19Z-
dc.date.available2022-07-09T18:06:19Z-
dc.date.created2021-05-12-
dc.date.issued2019-05-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/147913-
dc.description.abstractRecent progress in cellular reprogramming technology and lineage-specific cell differentiation has provided great opportunities for translational research. Because virus-based gene delivery is not a practical reprogramming protocol, protein-based reprogramming has been receiving attention as a safe way to generate reprogrammed cells. However, the poor efficiency of the cellular uptake of reprogramming proteins is still a major obstacle. Here, we reported key factors which improve the cellular uptake of these proteins. Purified red fluorescent proteins fused with 9xLysine (dsRED-9K) as a cell penetrating peptide were efficiently delivered into the diverse primary cells. Protein delivery was improved by the addition of amodiaquine. Furthermore, purified dsRED-9K was able to penetrate all cell lineages derived from mouse embryonic stem cells efficiently. Our data may provide important insights into the design of protein-based reprogramming or differentiation protocols.-
dc.language영어-
dc.language.isoen-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.titleEnhanced delivery of protein fused to cell penetrating peptides to mammalian cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Chang-Hwan-
dc.identifier.doi10.5483/BMBRep.2019.52.5.195-
dc.identifier.scopusid2-s2.0-85066494535-
dc.identifier.wosid000473211100005-
dc.identifier.bibliographicCitationBMB REPORTS, v.52, no.5, pp.324 - 329-
dc.relation.isPartOfBMB REPORTS-
dc.citation.titleBMB REPORTS-
dc.citation.volume52-
dc.citation.number5-
dc.citation.startPage324-
dc.citation.endPage329-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002467510-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusTAT PROTEIN-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusMODEL-
dc.subject.keywordAuthorAmodiaquine (AQ)-
dc.subject.keywordAuthorCell Penetrating Peptide (CPP)-
dc.subject.keywordAuthorDifferentiation-
dc.subject.keywordAuthorPolylysine (9K)-
dc.subject.keywordAuthorReprogramming-
dc.identifier.urlhttps://www.bmbreports.org/journal/view.html?doi=10.5483/BMBRep.2019.52.5.195-
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서울 의생명공학전문대학원 > 서울 의생명과학과 > 1. Journal Articles

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