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影响糖蛋白寡糖结构的生物工艺因素。

Bioprocess factors affecting glycoprotein oligosaccharide structure.

作者信息

Goochee C F

机构信息

Department of Chemical Engineering, Stanford University, CA 94305-5025.

出版信息

Dev Biol Stand. 1992;76:95-104.

PMID:1478360
Abstract

The oligosaccharide structures of glycoproteins can have a profound effect on properties critical to the development of glycoprotein products for human therapeutic or diagnostic use, including clearance rate, antigenicity, specific activity, solubility, resistance to thermal inactivation, and resistance to protease attack. Therefore, it is important to understand how bioprocess factors influence oligosaccharide structure. In this presentation, I will summarize literature data concerning potential effects of bioprocess factors on glycoprotein oligosaccharide biosynthesis. These data are drawn from two recent detailed reviews published by our laboratory describing the effect of cell culture conditions on N-linked glycosylation (10) and the effects of other bioprocess factors on both N-linked and O-linked glycosylation (11).

摘要

糖蛋白的寡糖结构可对用于人类治疗或诊断用途的糖蛋白产品开发的关键特性产生深远影响,这些特性包括清除率、抗原性、比活性、溶解度、耐热失活性以及抗蛋白酶攻击能力。因此,了解生物工艺因素如何影响寡糖结构很重要。在本报告中,我将总结有关生物工艺因素对糖蛋白寡糖生物合成潜在影响的文献数据。这些数据来自我们实验室最近发表的两篇详细综述,一篇描述细胞培养条件对N-连接糖基化的影响(10),另一篇描述其他生物工艺因素对N-连接和O-连接糖基化的影响(11)。

相似文献

1
Bioprocess factors affecting glycoprotein oligosaccharide structure.影响糖蛋白寡糖结构的生物工艺因素。
Dev Biol Stand. 1992;76:95-104.
2
The oligosaccharides of glycoproteins: bioprocess factors affecting oligosaccharide structure and their effect on glycoprotein properties.糖蛋白的寡糖:影响寡糖结构的生物工艺因素及其对糖蛋白性质的影响。
Biotechnology (N Y). 1991 Dec;9(12):1347-55. doi: 10.1038/nbt1291-1347.
3
Ammonium ion and glucosamine dependent increases of oligosaccharide complexity in recombinant glycoproteins secreted from cultivated BHK-21 cells.培养的BHK-21细胞分泌的重组糖蛋白中,铵离子和氨基葡萄糖依赖性增加寡糖复杂性。
Biotechnol Bioeng. 1998 Mar 5;57(5):518-28.
4
The third chains of living organisms--a trail of glycobiology that started from the third floor of building 4 in NIH.生物体的第三条链——一条始于美国国立卫生研究院4号楼三楼的糖生物学之路。
Arch Biochem Biophys. 2004 Jun 15;426(2):107-21. doi: 10.1016/j.abb.2004.01.023.
5
["Glyco-deglyco" processes during the biosynthesis of glycoproteins].糖蛋白生物合成过程中的“糖基化-去糖基化”过程
J Soc Biol. 1999;193(1):101-10.
6
Appropriate mammalian expression systems for biopharmaceuticals.适用于生物制药的哺乳动物表达系统。
Arzneimittelforschung. 1998 Aug;48(8):870-80.
7
Unusual uniformity of the N-linked oligosaccharides of HLA-A, -B, and -C glycoproteins.HLA - A、- B和 - C糖蛋白的N - 连接寡糖具有异常的一致性。
J Immunol. 1996 May 1;156(9):3275-84.
8
Comparison of biological activity among nonfucosylated therapeutic IgG1 antibodies with three different N-linked Fc oligosaccharides: the high-mannose, hybrid, and complex types.具有三种不同N-连接Fc寡糖(高甘露糖型、杂合型和复合型)的非岩藻糖基化治疗性IgG1抗体之间的生物学活性比较。
Glycobiology. 2007 Jan;17(1):104-18. doi: 10.1093/glycob/cwl057. Epub 2006 Sep 29.
9
N-glycosylation influences the latency and catalytic properties of mammalian purple acid phosphatase.N-糖基化影响哺乳动物紫色酸性磷酸酶的潜伏性和催化特性。
Arch Biochem Biophys. 2005 Mar 1;435(1):147-56. doi: 10.1016/j.abb.2004.11.029.
10
Structural characterization of oligosaccharides in recombinant soluble human interferon receptor 2 using fluorophore-assisted carbohydrate electrophoresis.利用荧光团辅助碳水化合物电泳对重组可溶性人干扰素受体2中的寡糖进行结构表征。
Electrophoresis. 2000 Jul;21(12):2296-308. doi: 10.1002/1522-2683(20000701)21:12<2296::AID-ELPS2296>3.0.CO;2-R.

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Optimisation of the cellular metabolism of glycosylation for recombinant proteins produced by Mammalian cell systems.优化哺乳动物细胞体系生产的重组蛋白的糖基化细胞代谢。
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Bovine acetylcholinesterase: cloning, expression and characterization.
牛乙酰胆碱酯酶:克隆、表达与特性分析
Biochem J. 1998 Aug 15;334 ( Pt 1)(Pt 1):251-9. doi: 10.1042/bj3340251.
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Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts.甘露糖可纠正碳水化合物缺乏糖蛋白综合征成纤维细胞中改变的 N-糖基化。
J Clin Invest. 1996 Mar 15;97(6):1478-87. doi: 10.1172/JCI118570.
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Involvement of oligomerization, N-glycosylation and sialylation in the clearance of cholinesterases from the circulation.寡聚化、N-糖基化和唾液酸化在胆碱酯酶从循环中清除过程中的作用。
Biochem J. 1995 Nov 1;311 ( Pt 3)(Pt 3):959-67. doi: 10.1042/bj3110959.