Unraveling the metabolism of HEK-293 cells using lactate isotopomer analysis

被引:36
作者
Henry, Olivier [1 ]
Jolicoeur, Mario [1 ]
Kamen, Amine [2 ]
机构
[1] Ecole Polytech, Dept Chem Engn, Montreal, PQ H3C 3A7, Canada
[2] Natl Res Council Canada, Biotechnol Res Inst, Montreal, PQ H4P 2R2, Canada
关键词
HEK-293; cells; Metabolism; C-13-metabolic flux analysis; Isotopic tracer; RECOMBINANT PROTEIN-PRODUCTION; TRANSIENT C-13-LABELING EXPERIMENTS; FLUX ANALYSIS; SERUM-FREE; GLUTAMINE-METABOLISM; ADENOVIRAL VECTORS; MURINE HYBRIDOMA; GENE-EXPRESSION; CULTURE PROCESS; BATCH CULTURES;
D O I
10.1007/s00449-010-0468-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
HEK-293 is the most extensively used human cell line for the production of viral vectors and is gaining increasing attention for the production of recombinant proteins by transient transfection. To further improve the metabolic characterization of this cell line, we have performed cultures using C-13-labeled substrates and measured the resulting mass isotopomer distributions in lactate by LC/MS. Simultaneous metabolite and isotopomer balancing allowed improvement and validation of the metabolic model and quantification of key intracellular pathways. We have determined the amounts of glucose carbon channeled through the PPP, incorporated into the TCA cycle for energy production and lipids biosynthesis, as well as the cytosolic and mitochondrial malic enzyme fluxes. Our analysis also revealed that glutamine did not significantly contribute to lactate formation. An improved and quantitative understanding of the central carbon metabolism is greatly needed to pursue the rational development of engineering approaches at both the cellular and process levels.
引用
收藏
页码:263 / 273
页数:11
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