期刊文献+

用高效廉价载体培养CHO细胞生产rHuEPO的研究 被引量:1

Production of rHuEPO via Culturing CHO Cells on High Efficient and Cheap Culture Carrier
在线阅读 下载PDF
导出
摘要 研究了以自制胶原蛋白载体及C-DISK载体培养CHO细胞生产rHuEPO蛋白的过程,并以进口A-DISK载体作为对照培养。对培养过程中细胞贴壁过程、葡萄糖代谢速率、rHuEPO浓度及葡萄糖代谢速率与rHuEPO的浓度变化关系进行了实验研究分析和对比。结果表明:自制胶原蛋白载体培养细胞具有良好的生物代谢活力和蛋白表达能力,葡萄糖代谢速率高达14.2mmol?mL?1?h?1,比自制C-DISK载体高16.4%,比进口A-DISK载体高12.7%;在自制胶原蛋白载体上培养CHO细胞时EPO表达量也最高,培养10天后EPO浓度达到282U?mL?1,比自制C-DISK载体高30%,也比进口A-DISK载体高18%。自制胶原蛋白载体具有较佳的性价比,是一种高效、廉价的动物细胞培养载体。细胞的葡萄糖代谢水平对蛋白表达有着重要的影响,但两者又不同步,因此可用葡萄糖的代谢速率变化对该培养过程和目的蛋白表达进行适当监测和调控。 The processes of culturing CHO(Chinese Hamster Ovary)cells to produce rHuEPO(recombinant human Erythropoietin)were investigated by using self-prepared collagen carrier, self-prepared C-DISK carrier and imported A-DISK carrier, respectively. The analysis and comparison of the anchorage of CHO cells, metabolic rates of glucose, expression concentration of rHuEPO and the relation between metabolic rate of glucose and expression concentration of rHuEPO for culturing CHO cells on three different carriers were experimentally carried out. The results show that self-prepared collagen carrier has the best bio-activity and highest protein expression in CHO cell culture. The maximum glucose metabolic rate of CHO cells cultured on self-prepared collagen carrier is as high as 14.2 mmol·mL^-1·h^-1,and which is 16.4% higher than that on C-DISK carrier, 12.8% higher than that on A-DISK carrier, the final rHuEPO expression concentration in CHO cell culture cultured on self-prepared collagen carriers reaches 282 U·mL^-1 after culturing ten days, and it is 30% higher than that on C-DISK carrier, 18% higher than that on A-DISK carrier. The self-prepared collagen carrier is a kind of high efficient and cheaper carrier which can be used for large-scale animal cell culture. The experimental results also show that the metabolic rate of glucose and expression concentration of rHuEPO in CHO cell culture cultured on different carriers are strongly relevant, but they are not in synchronization. This means that CHO cell culture stage can be detected and regulated by measuring the change of glucose metabolic rate.
出处 《高校化学工程学报》 EI CAS CSCD 北大核心 2005年第6期855-858,共4页 Journal of Chemical Engineering of Chinese Universities
基金 国家自然科学基金(20176018 20376034) 江苏省科技厅资助项目(BK2003084和BS2003030) 国家"十五"科技攻关项目(2004BA313B16)。
关键词 细胞培养 载体 CHO动物细胞 rHuEPO(重组人红细胞生长素) cell culture carrier CHO cells recombinant human Erythropoietin (rHuEPO)
  • 相关文献

参考文献8

  • 1XUYong-hua(徐永华).Engineering of Mammalian Cell Culture(动物细胞工程) [M].Beijing(北京): Chinese Chemical Industry Press(化,2003.2-10.
  • 2Boudreault P, Tremblay J P, Pepin M F. Scale-up of a myoblast culture process [J]. J Biotechnol, 2001,13: 63-74.
  • 3Felton L A, Garcia D I, Farmer R. Weight and weight uniformity of hard gelatin capsules filled with microcrystalline cellulose and silicified micro-crystalline cellulose [J]. Drug Dev Ind Pharm, 2002, 28: 467-472.
  • 4黄任远,胡云龙,沈树宝.胶原蛋白膜改性技术[J].南京工业大学学报(自然科学版),2004,26(4):23-26. 被引量:5
  • 5YUANQuan(袁权).Membrane separation and membrane reaction(膜分离和膜反应) [J].高校化学工程学报,1994,1:1-5.
  • 6ShanghaiKexinBioengLtd.(上海科欣生物工程有限公司).Instruction of GoD Enzymatic Glucose detection (GOD-酶法葡萄糖检测试剂盒使用说明书) [Z].,2002..
  • 7R & D Systems Inc. Quantikine IVD In Vitro Diagnosetic [Z]. Germany, 2003.
  • 8XUEQing-shan(薛庆善).Cell Culture Technology of in Vitro(体外细胞培养技术) [M].Beijing(北京): Chinese Medical Industry Press(医药,2003.643-661.

二级参考文献12

共引文献5

同被引文献11

  • 1高量,游磊,朱明龙,谭文松.rCHO细胞在葡萄糖限制流加培养过程中的生长与代谢特性[J].高校化学工程学报,2006,20(1):74-78. 被引量:14
  • 2Shukla A A,Th?mmes J. Recent advances in large-scale production of monoclonal antibodies and related proteins[J].{H}Trends in Biotechnology,2010,(05):253-261.
  • 3Chusainow J,Yang Y S,Yeo J H. A study of monoclonal antibody-producing CHO cell lines:What makes a stable high producer[J].{H}Biotechnology and Bioengineering,2009,(04):1182-1196.
  • 4Schr?der M,Matischak K,Friedl P. Serum-and protein-free media formulations for the Chinese hamster ovary cell line DUKXB11[J].{H}Journal of Biotechnology,2004,(03):279-292.
  • 5Burky J E,Wesson M C,Young A. Protein-free fed-batch culture of non-GS NS0 cell lines for production of recombinant antibodies[J].{H}Biotechnology and Bioengineering,2007,(02):281-293.
  • 6Altamirano C,IIIanes A,Canessa R. Specific nutrient supplementation of defined serum-free medium for the improvement of CHO cells growth and t-PA production[J].Electron J Biotechn,2006,(01):61-68.
  • 7de Zengotita V M,Abston L R,Schmelzer A E. Selected amino acids protect hybridoma and CHO cells from elevated carbon dioxide and osmolality[J].{H}Biotechnology and Bioengineering,2002,(07):741-752.
  • 8Franěk F,?rámková K. Cell suicide in starving hybridoma culture Survival signal effect of amino acid[J].{H}CYTOTECHNOLOGY,1997,(01):231-239.
  • 9Oyaas K,Ellingsen T E,Dyrset N. Utilization of osmoprotective compounds by hybridoma cells exposed to hyperosmotic stress[J].{H}Biotechnology and Bioengineering,1994,(01):77-89.
  • 10Ishaque A,Al-Rubeai M. Role of vitamins in determining apoptosis and extent of suppression by bcl-2 during hybridoma cell culture[J].{H}APOPTOSIS,2002,(03):231-239.

引证文献1

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部