Identification of Cell Culture Conditions to Control N-Glycosylation Site-Occupancy of Recombinant Glycoproteins Expressed in CHO Cells

被引:77
作者
Gawlitzek, Martin [1 ,2 ]
Estacio, Michael [1 ,3 ]
Fuerch, Tobias [1 ]
Kiss, Robert [1 ,2 ]
机构
[1] Genentech Inc, Mfg Sci & Technol, San Francisco, CA 94080 USA
[2] Genentech Inc, Proc Res & Dev, Late Stage Cell Culture, San Francisco, CA 94080 USA
[3] Genentech Inc, Prod Technol, Automat & Prod Informat Technol, San Francisco, CA 94080 USA
关键词
CHO cells; glycosylation; site-occupancy; sialic acid; cell culture; HAMSTER OVARY CELLS; INTERFERON-GAMMA GLYCOSYLATION; PLASMINOGEN-ACTIVATOR; SODIUM-BUTYRATE; OLIGOSACCHARYL TRANSFERASE; GLYCOSIDASE ACTIVITIES; PROTEIN GLYCOSYLATION; SECRETORY PATHWAY; ERYTHROPOIETIN; TEMPERATURE;
D O I
10.1002/bit.22348
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
The effect of different Cell Culture conditions on N-glycosylation site-occupancy has been elucidated for two different recombinant glycoproteins expressed in Chinese hamster ovary (CHO) cells, recombinant human tissue plasminogen activator (t-PA) and a recombinant enzyme (glycoprotein 2-GP2). Both molecules contain a N-glycosylation site that is variably occupied. Different environmental factors that affect the site-occupancy (the degree of occupied sites) of these molecules were identified. Supplementing the culture medium with additional manganese or iron, increased the fraction of hilly occupied t-PA (type I t-PA) by approximately 2.5-4%. Decreasing the cultivation temperature from 37 to 33 degrees C or 31 degrees C gradually increased site-occupancy of t-PA up to 4%. The addition of a specific productivity enhancer, butyrate, further increased site-occupancy by an additional 1% under each cultivation temperature tested. In addition, the thyroid hormones triiodothyronine and thyroxine increased site-occupancy of t-PA compared to control conditions by about 2%. In contrast, the addition of relevant nucleoside precursor molecules involved in N-glycan biosynthesis (e.g., uridine, guanosine, mannose) either had no effect or slightly reduced site-occupancy. For the recombinant enzyme (GP2), it was discovered that Culture pH and the timing of butyrate addition can be used to control N-glycan site-occupancy within a specific range. An increase in culture pH correlated with a decrease in site-occupancy. Similarly, delaying the timing for butyrate addition also decreased site-occupancy of this molecule. These results highlight the importance of understanding how cell culture conditions and media components can affect the product quality of recombinant glycoproteins expressed in mammalian cell cultures. Furthermore, the identification of relevant factors will enable one to control product quality attributes, specifically N-glycan site-occupancy, within a specific range when applied appropriately. Biotechnol. Bioeng. 2009;103: 1164-1175. (C) 2009 Wiley Periodicals, Inc.
引用
收藏
页码:1164 / 1175
页数:12
相关论文
共 55 条
[41]   ROLE OF EXTRACELLULAR SIGNALING ON ENDOTHELIAL-CELL PROLIFERATION AND PROTEIN N-GLYCOSYLATION [J].
OLIVEIRA, CM ;
BANERJEE, DK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 144 (03) :467-472
[42]   EFFECT OF MEDIUM OSMOLARITY ON HYBRIDOMA GROWTH, METABOLISM, AND ANTIBODY-PRODUCTION [J].
OZTURK, SS ;
PALSSON, BO .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 37 (10) :989-993
[43]   Expression cloning of cDNA encoding a human β-1,3-N-acetylglucosaminyltransferase that is essential for poly-N-acetyllactosamine synthesis [J].
Sasaki, K ;
Kurata-Miura, K ;
Ujita, M ;
Angata, K ;
Nakagawa, S ;
Sekine, S ;
Nishi, T ;
Fukuda, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14294-14299
[44]   The importance of ammonia in mammalian cell culture [J].
Schneider, M ;
Marison, IW ;
vonStockar, U .
JOURNAL OF BIOTECHNOLOGY, 1996, 46 (03) :161-185
[45]  
Shelikoff M, 1996, BIOTECHNOL BIOENG, V50, P73, DOI 10.1002/(SICI)1097-0290(19960405)50:1<73::AID-BIT9>3.0.CO
[46]  
2-Z
[47]  
SPEARMAN M, 2005, CELL TECHNOLOGY PROD, P71
[48]   Identification of genes responsive to sodium butyrate in colonic epithelial cells [J].
Tabuchi, Y ;
Arai, Y ;
Kondo, T ;
Takeguchi, N ;
Asano, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 293 (04) :1287-1294
[49]   Process parameter shifting:: Part I.: Effect of DOT, pH, and temperature on the performance of Epo-Fc expressing CHO cells cultivated in controlled batch bioreactors [J].
Trummer, Evelyn ;
Fauland, Katharina ;
Seidinger, Silke ;
Schriebl, Kornelia ;
Lattenmayer, Christine ;
Kunert, Renate ;
Vorauer-Uhl, Karola ;
Weik, Robert ;
Borth, Nicole ;
Katinger, Hermann ;
Mueller, Dethardt .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 94 (06) :1033-1044
[50]   ISOLATION OF CHINESE-HAMSTER CELL MUTANTS DEFICIENT IN DIHYDROFOLATE-REDUCTASE ACTIVITY [J].
URLAUB, G ;
CHASIN, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :4216-4220