Genetic optimization of recombinant glycoprotein production by mammalian cells

被引:89
作者
Fussenegger, M [1 ]
Bailey, JE
Hauser, H
Mueller, PP
机构
[1] ETH Honggerberg, Inst Biotechnol, HPT, CH-8093 Zurich, Switzerland
[2] GBF, Natl Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany
关键词
D O I
10.1016/S0167-7799(98)01248-7
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
Genetically modified mammalian cells are the preferred system for the production of recombinant therapeutic glycoproteins. Other applications include engineering of cell lines for drug screening and cell-based therapies, and the construction of recombinant viruses for gene therapy. This article highlights contemporary core genetic technologies and emerging strategies for genetically engineering mammalian cells for optimal recombinant-protein expression.
引用
收藏
页码:35 / 42
页数:8
相关论文
共 124 条
[1]   SPECIFIC MONOCLONAL-ANTIBODY PRODUCTIVITY AND THE CELL CYCLE-COMPARISONS OF BATCH, CONTINUOUS AND PERFUSION CULTURES [J].
ALRUBEAI, M ;
EMERY, AN ;
CHALDER, S ;
JAN, DC .
CYTOTECHNOLOGY, 1992, 9 (1-3) :85-97
[2]   DEATH MECHANISMS OF ANIMAL-CELLS IN CONDITIONS OF INTENSIVE AGITATION [J].
ALRUBEAI, M ;
SINGH, RP ;
GOLDMAN, MH ;
EMERY, AN .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 45 (06) :463-472
[3]  
Bailey JE, 1997, ANIMAL CELL TECHNOLOGY, P489
[4]   TOWARD A SCIENCE OF METABOLIC ENGINEERING [J].
BAILEY, JE .
SCIENCE, 1991, 252 (5013) :1668-1675
[5]  
BAILEY JE, 1998, NEW DEV NEW APPL ANI, P5
[6]   COREGULATION OF 2 GENE ACTIVITIES BY TETRACYCLINE VIA A BIDIRECTIONAL PROMOTER [J].
BARON, U ;
FREUNDLIEB, S ;
GOSSEN, M ;
BUJARD, H .
NUCLEIC ACIDS RESEARCH, 1995, 23 (17) :3605-3606
[7]   SEMLIKI FOREST VIRUS EXPRESSION SYSTEM - PRODUCTION OF CONDITIONALLY INFECTIOUS RECOMBINANT PARTICLES [J].
BERGLUND, P ;
SJOBERG, M ;
GAROFF, H ;
ATKINS, GJ ;
SHEAHAN, BJ ;
LILJESTROM, P .
BIO-TECHNOLOGY, 1993, 11 (08) :916-920
[8]   Scaffold/matrix-attached regions: Topological switches with multiple regulatory functions [J].
Bode, J ;
StengertIber, M ;
Kay, V ;
Schlake, T ;
DietzPfeilstetter, A .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 1996, 6 (2-3) :115-138
[9]  
Bode J, 1995, INT REV CYTOL, V162A, P389
[10]   Comparison of picornaviral IRES-driven internal initiation of translation in cultured cells of different origins [J].
Borman, AM ;
LeMercier, P ;
Girard, M ;
Kean, KM .
NUCLEIC ACIDS RESEARCH, 1997, 25 (05) :925-932