Comprehensive Analysis of Genomic Safe Harbors as Target Sites for Stable Expression of the Heterologous Gene in HEK293 Cells

被引:24
|
作者
Shin, Seunghyeon [2 ]
Kim, Su Hyun [2 ]
Shin, Sung Wook [1 ]
Grav, Lise Marie [3 ]
Pedersen, Lasse Ebdrup [3 ]
Lee, Jae Seong [1 ]
Lee, Gyun Min [2 ,3 ]
机构
[1] Ajou Univ, Dept Mol Sci & Technol, Suwon 16499, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 305701, South Korea
[3] Tech Univ Denmark, Novo Nordisk Fdn Ctr Biosustainabil, DK-2800 Lyngby, Denmark
来源
ACS SYNTHETIC BIOLOGY | 2020年 / 9卷 / 06期
基金
新加坡国家研究基金会;
关键词
CRISPR/Cas9; genomic safe harbor; HEK cells; recombinase-mediated cassette exchange; site-specific integration; therapeutic protein; HAMSTER OVARY CELLS; INTEGRATION; DNA; PLATFORMS; STABILITY; ABSENCE; LOCUS;
D O I
10.1021/acssynbio.0c00097
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human cell lines are being increasingly used as host cells to produce therapeutic glycoproteins, due to their human glycosylation machinery. In an attempt to develop a platform for generating isogenic human cell lines producing therapeutic proteins based on targeted integration, three well-known human genomic safe harbors (GSHs)-AAVS1, CCRS, and human ROSA26 loci-were evaluated with respect to the transgene expression level and stability in human embryonic kidney (HEK293) cells. Among the three GSHs, the AAVS1 locus showed the highest eGFP expression with the highest homogeneity. Transgene expression at the AAVS1 locus was sustained without selection for approximately 3 months. Furthermore, the CMV promoter showed the highest expression, followed by the EF1 alpha, SV40, and TK promoters at the AAVS1 locus. Master cell lines were created using CRISPR/Cas9-mediated integration of the landing pad into the AAVS1 locus and were used for faster generation of recombinant cell lines that produce therapeutic proteins with recombinase-mediated cassette exchange.
引用
收藏
页码:1263 / 1269
页数:7
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