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Enhanced delivery of protein fused to cell penetrating peptides to mammalian cellsopen access

Authors
Moon, Jung-IlHan, Min-JoonYu, Shin-HyeLee, Eun-HyeKim, Sang-MiHan, KyuboemPark, Chang-HwanKim, Chun-Hyung
Issue Date
May-2019
Publisher
KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
Keywords
Amodiaquine (AQ); Cell Penetrating Peptide (CPP); Differentiation; Polylysine (9K); Reprogramming
Citation
BMB REPORTS, v.52, no.5, pp.324 - 329
Indexed
SCIE
SCOPUS
KCI
Journal Title
BMB REPORTS
Volume
52
Number
5
Start Page
324
End Page
329
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/147913
DOI
10.5483/BMBRep.2019.52.5.195
ISSN
1976-6696
Abstract
Recent 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.
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서울 의생명공학전문대학원 > 서울 의생명과학과 > 1. Journal Articles

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