Combination of FACS and Homologous Recombination for the Generation of Stable and High-Expression Engineered Cell Lines
Science
Genetic Vectors
Green Fluorescent Proteins
Gene Expression
CHO Cells
Transfection
Receptors, Tumor Necrosis Factor
Etanercept
03 medical and health sciences
Cricetulus
Animals
Transgenes
Selection, Genetic
Homologous Recombination
Cell Engineering
0303 health sciences
Q
R
Flow Cytometry
Founder Effect
Clone Cells
Electroporation
Immunoglobulin G
Medicine
Research Article
DOI:
10.1371/journal.pone.0091712
Publication Date:
2014-03-19T22:48:10Z
AUTHORS (7)
ABSTRACT
Traditionally, cell line generation requires several months and involves screening of over several hundred cell clones for high productivity before dozens are selected as candidate cell lines. Here, we have designed a new strategy for the generation of stable and high-expression cell lines by combining homologous recombination (HR) and fluorescence-activated cell sorting (FACS). High expression was indicated by the expression of secreted green fluorescent protein (SEGFP). Parental cell lines with the highest expression of SEGFP were then selected by FACS and identified by stability analysis. Consequently, HR vectors were constructed using the cassette for SEGFP as the HR region. After transfecting the HR vector, the cells with negative SEGFP expression were enriched by FACS. The complete exchange between SEGFP and target gene (TNFR-Fc) cassettes was demonstrated by DNA analysis. Compared with the traditional method, by integrating the cassette containing the gene of interest into the pre-selected site, the highest producing cells secreted a more than 8-fold higher titer of target protein. Hence, this new strategy can be applied to isolated stable cell lines with desirable expression of any gene of interest. The stable cell lines can rapidly produce proteins for researching protein structure and function and are even applicable in drug discovery.
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