Proteomic profiling of CHO cells with enhanced rhBMP-2 productivity following co-expression of PACEsol
Autor: | Linda Francullo, Martin S. Sinacore, Mark Melville, Paula Meleady, Timothy S. Charlebois, Padraig Doolan, Michael Henry, Mark Leonard, Martin Clynes, Patrick Gammell |
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Rok vydání: | 2008 |
Předmět: |
Proteomics
Proteome Cell Culture Techniques Bone Morphogenetic Protein 2 Gene Expression CHO Cells Biology Transfection Peptide Mapping Biochemistry Bone morphogenetic protein 2 Cell Line Cricetulus Transforming Growth Factor beta Cricetinae Animals Humans Electrophoresis Gel Two-Dimensional Molecular Biology Furin Proteomic Profiling Gene Expression Profiling Chinese hamster ovary cell Recombinant Proteins Clone Cells Gene expression profiling Cell culture Spectrometry Mass Matrix-Assisted Laser Desorption-Ionization Bone Morphogenetic Proteins Dimerization |
Zdroj: | PROTEOMICS. 8:2611-2624 |
ISSN: | 1615-9861 1615-9853 |
Popis: | Chinese hamster ovary (CHO) cells are widely used for the production of recombinant protein biopharmaceuticals. The purpose of this study was to investigate differences in the proteome of CHO DUKX cells expressing recombinant human bone morphogenetic protein-2 (rhBMP-2) (G5 cells) compared to cells also expressing soluble exogenous paired basic amino acid cleaving enzyme soluble paired basic amino acid cleaving enzyme (PACEsol) (3C9 cells), which has been previously found to improve the post-translational processing of the mature rhBMP-2 dimer. PACEsol co-expression was also associated with a significant increase (almost four-fold) in cellular productivity of rhBMP-2 protein. Differential proteomic expression profiling using 2-D DIGE and MALDI-TOF MS was performed to compare 3C9 and G5 cells, and revealed a list of 60 proteins that showed differential expression (up/downregulated), with a variety of different cellular functions. A substantial number of these altered proteins were found to have chaperone activity, involved with protein folding, assembly and secretion, as well as a number of proteins involved in protein translation. These results support the use of proteomic profiling as a valuable tool towards understanding the biology of bioprocess cultures. |
Databáze: | OpenAIRE |
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