scholarly journals Targeted genetic modification of cell lines for recombinant protein production

2007 ◽  
Vol 53 (1-3) ◽  
pp. 65-73 ◽  
Author(s):  
Niall Barron ◽  
Olga Piskareva ◽  
Mohan Muniyappa
2018 ◽  
Vol 73 (3-4) ◽  
pp. 147-151
Author(s):  
Xiaoli Ju ◽  
Meijia Ren ◽  
Keping Chen ◽  
Qiang Wang

AbstractDue to their numerous advantages, baculovirus expression vector systems (BEVS) have been widely used to express recombinant proteins for different purposes. Different strategies have been adopted to increase recombinant protein production. In this study, we transiently or stably expressed mousec-Mycin High Five cells using a commercial pIB/V5 vector. Under the control of theOpIE2promoter, this vector could enhance recombinant protein production. We found that transient expression ofc-Mycin High Five cells improved recombinant protein production. Furthermore, we established two stable cell lines, High Five-c-Myc #1 and High Five-c-Myc #2, that stably expressed mousec-Myc. We further found that the expression level of the recombinant protein was increased in these stable cell lines compared to control cell lines. These data indicate that overexpressingc-Mycin cells is a promising way to improve recombinant protein production in BEVS.


2015 ◽  
Vol 9 (S9) ◽  
Author(s):  
Emilie Vaxelaire ◽  
Lauriane Gamand ◽  
Christel Aebischer-Gumy ◽  
Pierre Moretti ◽  
Martin Bertschinger

2020 ◽  
Author(s):  
Rasool Saghaleyni ◽  
Magdalena Malm ◽  
Jan Zrimec ◽  
Ronia Razavi ◽  
Num Wistbacka ◽  
...  

SummaryHigher eukaryotic cell lines like HEK293 are the preferred hosts for production of therapeutic proteins requiring human post translational processing. However, recombinant protein production can result in severe stress on the cellular machinery, resulting in limited titre and product quality. To investigate the cellular and metabolic characteristics associated with these limitations, we compared erythropoietin (secretory) and GFP (non-secretory) protein producer HEK293 cell-lines using transcriptomics analysis. Despite the high demand for ATP in all protein producer clones, a significantly higher capacity for ATP production was observed with erythropoietin producers as evidenced by the enrichment of upregulated genes in the oxidative phosphorylation pathway. In addition, ribosomal genes exhibited specific patterns of expression depending on the recombinant protein and the production rate. In a clone displaying a dramatically increased erythropoietin secretion, we detected higher ER stress, including upregulation of the ATF6B gene. Our results are significant in recognizing key pathways for recombinant protein production and identifying potential target genes for further development of secretory power in mammalian cell factories.In BriefAlthough the protein secretion process has been widely studied, the complexity of it leaves many questions with regards to defining bottlenecks for successful protein secretion to be answered. By investigating the transcriptomic profiles of different HEK293 clones with varying translational rates producing either the secreted protein erythropoietin or the intracellular GFP, we reveal that high ATP production and improved capacity of specific post-translational pathways are key factors associated with boosting erythropoietin production.HighlightsTranscriptomics analysis of a panel of HEK293 stable cell lines expressing GFP or erythropoietin (EPO) at varying translational ratesExpression of mitochondrial ribosomal genes is positively correlated with EPO secretionExpression of different cytosolic ribosomal genes are correlated with productivity in a recombinant-protein specific mannerHigh EPO producing clones have significant upregulation of ATF6B, potentially enabling a beneficial ER stress response to cope with high protein secretionGraphical Abstract


1993 ◽  
Vol 29 (5) ◽  
pp. 388-390 ◽  
Author(s):  
T. R. Davis ◽  
T. J. Wickham ◽  
K. A. McKenna ◽  
R. R. Granados ◽  
M. L. Shuler ◽  
...  

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