A GFP-based method facilitates clonal selection of transfected CHO cells

被引:15
|
作者
Freimark, Denise [1 ]
Jerome, Valerie [1 ]
Freitag, Ruth [1 ]
机构
[1] Univ Bayreuth, Chair Proc Biotechnol, D-95440 Bayreuth, Germany
关键词
Growth factor; High producer; Mammalian cell culture; Recombinant protein production; Transfection; GREEN FLUORESCENT PROTEIN; EXPRESSION; GROWTH; OPTIMIZATION;
D O I
10.1002/biot.200800264
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The identification of highly expressing clones is a crucial step in the development of cell lines for production of recombinant proteins. Here we present a method based on the co-expression of enhanced green fluorescent protein (EGFP) that allows clonal selection in standard 96-well cell culture plates. The genes encoding the EGFP protein and the protein of interest are linked by an internal ribosome entry site and thus are transcribed into the same mRNA but are translated independently. Since both proteins arise from a common mRNA, the EGFP expression level correlates with the expression level of the therapeutic protein for each clone. By expressing recombinant growth factors in CHO cells, we demonstrate the robustness and performance of this technique. The method is an alternative to the identification of high-producer clones using various cell sorting methods, as it can be performed with standard laboratory equipment.
引用
收藏
页码:24 / 31
页数:8
相关论文
共 50 条
  • [21] Thrombin facilitates sodium channel activation in freshly isolated human cardiomyocytes but not in CHO cells transfected with h Nav1.5
    Le Grand, B
    Leparq, A
    Pinet, C
    Coulombe, A
    Wurch, T
    John, G
    EUROPEAN HEART JOURNAL, 2003, 24 : 507 - 507
  • [22] Enhancer-specified GFP-based FACS purification of human spinal motor neurons from embryonic stem cells
    Roy, NS
    Nakano, T
    Xuing, L
    Kang, J
    Nedergaard, M
    Goldman, SA
    EXPERIMENTAL NEUROLOGY, 2005, 196 (02) : 224 - 234
  • [23] Green fluorescent protein as a second selectable marker for selection of high producing clones from transfected CHO cells
    Meng, YG
    Liang, J
    Wong, WL
    Chisholm, V
    GENE, 2000, 242 (1-2) : 201 - 207
  • [24] Myosin-actin Interaction in Dictyostelium Cells Revealed by GFP-based Strain Sensor and Validated Linear Spectral Unmixing
    Iwai, Sosuke
    Uyeda, Taro Q. P.
    CYTOMETRY PART A, 2010, 77A (08) : 743 - 750
  • [25] Growth kinetic studies (in hours) based on the fluorescence of stable, GFP-expressing CHO cells
    Hunt, L
    Jordan, M
    De Jesus, M
    Wurm, FM
    ANIMAL CELL TECHNOLOGY: PRODUCTS FROM CELLS, CELLS AS PRODUCTS, 1999, : 119 - 121
  • [26] Development and application of a GFP-based FRET probe for detecting caspase3 activation during apoptosis in living HeLa cells
    Luo, KQ
    Yu, V
    Pu, YM
    Chang, DD
    MOLECULAR BIOLOGY OF THE CELL, 2000, 11 : 255A - 255A
  • [27] A novel clonal selection algorithm based fragile watermarking method
    Aslantas, Veysel
    Ozer, Saban
    Ozturk, Serkan
    ARTIFICIAL IMMUNE SYSTEMS, PROCEEDINGS, 2007, 4628 : 358 - +
  • [28] The Common MUTYH Variant Q324H Has Reduced OG: A Lesion Repair in a GFP-Based Assay in Mammalian Cells
    Raetz, A. G.
    Xie, Y.
    Chang, C.
    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2011, 52 : S43 - S43
  • [29] High-throughput clonal selection of antibody-producing CHO cells using a microfluidic cell culture platform
    Lecault, Veronique
    Bowden, William J.
    Verma, Anjali
    Singhal, Anupam
    Orlando, Joe
    Martin, Christopher
    Piret, James M.
    Hansen, Carl L.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [30] OPTIMIZATION METHOD BASED ON THE SYNTHESIS OF CLONAL SELECTION AND ANNEALING SIMULATION ALGORITHMS
    Grygor, O. O.
    Fedorov, E. E.
    Utkina, T. Yu
    Lukashenko, A. G.
    Rudakov, K. S.
    Harder, D. A.
    Lukashenko, V. M.
    RADIO ELECTRONICS COMPUTER SCIENCE CONTROL, 2019, (02) : 90 - 99