Fundamentals of Expression in Mammalian Cells

被引:27
作者
Dyson, Michael R. [1 ]
机构
[1] IONTAS Ltd, Babraham Res Campus, Cambridge CB22 3AT, England
来源
ADVANCED TECHNOLOGIES FOR PROTEIN COMPLEX PRODUCTION AND CHARACTERIZATION | 2016年 / 896卷
关键词
Antibody expression; Biologics production; Transient transfection; High-throughput expression; RECOMBINANT PROTEIN-PRODUCTION; TRANSIENT GENE-EXPRESSION; EPSTEIN-BARR-VIRUS; HIGH-LEVEL; STEM-CELLS; TRANSFECTION; VECTORS; LINES; ANTIBODIES; SYSTEM;
D O I
10.1007/978-3-319-27216-0_14
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of proteins in mammalian cells is a key technology important for many functional studies on human and higher eukaryotic genes. Studies include the mapping of protein interactions, solving protein structure by crystallization and X-ray diffraction or solution phase NMR and the generation of antibodies to enable a range of studies to be performed including protein detection in vivo. In addition the production of therapeutic proteins and antibodies, now a multi billion dollar industry, has driven major advances in cell line engineering for the production of grams per liter of active proteins and antibodies. Here the key factors that need to be considered for successful expression in HEK293 and CHO cells are reviewed including host cells, expression vector design, transient transfection methods, stable cell line generation and cultivation conditions.
引用
收藏
页码:217 / 224
页数:8
相关论文
共 53 条
  • [1] Better and faster: improvements and optimization for mammalian recombinant protein production
    Almo, Steven C.
    Love, James D.
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2014, 26 : 39 - 43
  • [2] Rational vector design and multi-pathway modulation of HEK 293E cells yield recombinant antibody titers exceeding 1 g/l by transient transfection under serum-free conditions
    Backliwal, Gaurav
    Hildinger, Markus
    Chenuet, Sebastien
    Wulhfard, Sarah
    De Jesus, Maria
    Wurm, Florian M.
    [J]. NUCLEIC ACIDS RESEARCH, 2008, 36 (15)
  • [3] Rapid recombinant protein production from piggyBac transposon-mediated stable CHO cell pools
    Balasubramanian, Sowmya
    Matasci, Mattia
    Kadlecova, Zuzana
    Baldi, Lucia
    Hacker, David L.
    Wurm, Florian M.
    [J]. JOURNAL OF BIOTECHNOLOGY, 2015, 200 : 61 - 69
  • [4] Stable mammalian producer cell lines for structural biology
    Buessow, Konrad
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2015, 32 : 81 - 90
  • [5] Sialic acids: carbohydrate moieties that influence the biological and physical properties of biopharmaceutical proteins and living cells
    Byrne, Barry
    Donohoe, Gerard G.
    O'Kennedy, Richard
    [J]. DRUG DISCOVERY TODAY, 2007, 12 (7-8) : 319 - 326
  • [6] CACHIANES G, 1993, BIOTECHNIQUES, V15, P255
  • [7] Chapple SD, 2014, METHODS MOL BIOL, V1091, P143, DOI 10.1007/978-1-62703-691-7_9
  • [8] Multiplexed expression and screening for recombinant protein production in mammalian cells
    Chapple, Susan D. J.
    Crofts, Anna M.
    Shadbolt, S. Paul
    McCafferty, John
    Dyson, Michael R.
    [J]. BMC BIOTECHNOLOGY, 2006, 6 (1)
  • [9] A High-Yielding CHO Transient System: Coexpression of Genes Encoding EBNA-1 and GS Enhances Transient Protein Expression
    Daramola, Olalekan
    Stevenson, Jessica
    Dean, Greg
    Hatton, Diane
    Pettman, Gary
    Holmes, William
    Field, Ray
    [J]. BIOTECHNOLOGY PROGRESS, 2014, 30 (01) : 132 - 141
  • [10] Import of plasmid DNA into the nucleus is sequence specific
    Dean, DA
    [J]. EXPERIMENTAL CELL RESEARCH, 1997, 230 (02) : 293 - 302