生物
异源表达
HEK 293细胞
异源的
基因
遗传学
基因表达
计算生物学
重组DNA
作者
Seunghyeon Shin,Su-Hyun Kim,Sung-Wook Shin,Lise Marie Grav,Lasse Ebdrup Pedersen,Jae Seong Lee,Gyun‐Min Lee,Seunghyeon Shin,Su-Hyun Kim,Sung-Wook Shin,Lise Marie Grav,Lasse Ebdrup Pedersen,Jae Seong Lee,Gyun‐Min Lee
标识
DOI:10.1021/acssynbio.0c00097
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, CCR5, 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 EF1α, 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.
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