Expression systems for therapeutic glycoprotein production

被引:273
作者
Durocher, Yves [1 ]
Butler, Michael [2 ]
机构
[1] Natl Res Council Canada, Biotechnol Res Inst, Anim Cell Technol Grp, Montreal, PQ H4P 2R2, Canada
[2] Univ Manitoba, Dept Microbiol, Winnipeg, MB R3T 2N2, Canada
关键词
HAMSTER OVARY CELLS; INTERFERON-GAMMA PRODUCTION; HUMAN MONOCLONAL-ANTIBODY; SIALIC ACID TRANSPORTER; RECOMBINANT FACTOR-VIII; CHO-CELLS; PROTEIN-PRODUCTION; OVER-EXPRESSION; GLYCOSYLATION PATHWAY; HYPOTHERMIC GROWTH;
D O I
10.1016/j.copbio.2009.10.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There are slightly over 165 recombinant pharmaceuticals currently approved for human use. Another 500 protein candidates are in preclinical and clinical development, about 70% of these being glycosylated proteins. The need for expression systems allowing the efficient manufacturing of high quality glycoproteins is thus becoming imperative. Recent developments with CHO cells, the predominant mammalian expression system, have focused on either increasing cell specific productivity or prolonging the life span of cells in culture that translates to high integrated viable cell densities. These two factors have allowed volumetric productivities in excess of 5 g/L under conditions of controlled nutrient feeding. In addition to glycoengineering strategies, which are offering considerable advantage in producing proteins with enhanced therapeutic properties, several alternative expression systems are being developed for their manufacture, each with their advantages and limitations.
引用
收藏
页码:700 / 707
页数:8
相关论文
共 93 条
[1]   Correlation of DNA methylation with histone modifications across the HNRPA2B1-CBX3 ubiquitously-acting chromatin open element (UCOE) [J].
Allen, Marianne Lindahl ;
Antoniou, Michael .
EPIGENETICS, 2007, 2 (04) :227-236
[2]   Identification of novel small molecule enhancers of protein production by cultured mammalian cells [J].
Allen, Martin J. ;
Boyce, James P. ;
Trentalange, Michael T. ;
Treiber, David L. ;
Rasmussen, Brian ;
Tillotson, Benjamin ;
Davis, Raymond ;
Reddy, Pranhitha .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 100 (06) :1193-1204
[3]   The impact of glycosylation on the biological function and structure of human immunoglobulins [J].
Arnold, James N. ;
Wormald, Mark R. ;
Sim, Robert B. ;
Rudd, Pauline M. ;
Dwek, Raymond A. .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :21-50
[4]   Trends in Glycosylation, Glycoanalysis and Glycoengineering of Therapeutic Antibodies and Fc-Fusion Proteins [J].
Beck, Alain ;
Wagner-Rousset, Elsa ;
Bussat, Marie-Claire ;
Lokteff, Maryline ;
Klinguer-Hamour, Christine ;
Haeuw, Jean-Francois ;
Goetsch, Liliane ;
Wurch, Thierry ;
Van Dorsselaer, Alain ;
Corvaia, Nathalie .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2008, 9 (06) :482-501
[5]   An XBP-1 dependent bottle-neck in production of IgG subtype antibodies in chemically defined serum-free Chinese hamster ovary (CHO) fed-batch processes [J].
Becker, Eric ;
Florin, Lore ;
Pfizenmaier, Klaus ;
Kaufmann, Hitto .
JOURNAL OF BIOTECHNOLOGY, 2008, 135 (02) :217-223
[6]   Comparison of recombinant and plasma-derived antithrombin biodistribution in a rabbit model [J].
Berry, Leslie R. ;
Thong, Bruce ;
Chan, Anthony K. C. .
THROMBOSIS AND HAEMOSTASIS, 2009, 102 (02) :302-308
[7]   Short-hairpin-RNA-mediated silencing of fucosyltransferase 8 in Chinese-hamster ovary cells for the production of antibodies with enhanced antibody immune effector function [J].
Beuger, Vincent ;
Kuenkele, Klaus-Peter ;
Koll, Hans ;
Gaertner, Achim ;
Baehner, Monika ;
Burtscher, Helmut ;
Klein, Christian .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2009, 53 :31-37
[8]   Uncoupling of cell growth and proliferation results in enhancement of productivity in p21C1P1-arrested CHO cells [J].
Bi, JX ;
Shuttleworth, J ;
Ai-Rubeai, M .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 85 (07) :741-749
[9]   Bioproduction of therapeutic proteins in the 21st century and the role of plants and plant cells as production platforms [J].
Boehm, Robert .
BIOLOGY OF EMERGING VIRUSES: SARS, AVIAN AND HUMAN INFLUENZA, METAPNEUMOVIRUS, NIPAH, WEST NILE, AND ROSS RIVER VIRUS, 2007, 1102 :121-134
[10]   Increasing the Sialylation of Therapeutic Glycoproteins: The Potential of the Sialic Acid Biosynthetic Pathway [J].
Bork, Kaya ;
Horstkorte, Ruediger ;
Weidemann, Wenke .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (10) :3499-3508