Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

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

Full metadata record
DC Field Value Language
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-
Files in This Item
Appears in
Collections
서울 의생명공학전문대학원 > 서울 의생명과학과 > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Park, Chang Hwan photo

Park, Chang Hwan
GRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING (DEPARTMENT OF BIOMEDICAL SCIENCE)
Read more

Altmetrics

Total Views & Downloads

BROWSE