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Improving expression of recombinant human IGF‐1 using IGF‐1R knockout CHO cell lines
Author(s) -
Romand Sandrine,
Jostock Thomas,
Fornaro Mara,
Schmidt Joerg,
Ritter Anett,
Wilms Burkhard,
Laux Holger
Publication year - 2016
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.25877
Subject(s) - chinese hamster ovary cell , cell culture , recombinant dna , cell growth , biology , transfection , clone (java method) , cricetulus , microbiology and biotechnology , gene knockout , growth factor , receptor , gene , biochemistry , genetics
Chinese Hamster Ovary (CHO) cells are widely used for the large‐scale production of recombinant biopharmaceuticals. However, attempts to express IGF‐1 (a mutated human Insulin‐like growth factor 1 Ea peptide (hIGF‐1Ea mut)) in CHO cells resulted in poor cell growth and low productivity (0.1–0.2 g/L). Human IGF‐1 variants negatively impacted CHO cell growth via the IGF‐1 receptor (IGF‐1R). Therefore knockout (KO) of the IGF‐1R gene in two different CHO cell lines as well as knockdown (KD) of IGF‐1R in one CHO cell line were performed. These cell line engineering approaches decreased significantly the hIGF‐1 mediated cell growth inhibition and increased productivity of both KO CHO cell lines as well as of the KD CHO cell line. A productivity increase of 10‐fold at pool level and sevenfold at clone level was achieved, resulting in a titer of 1.3 g/L. This data illustrate that cell line engineering approaches are powerful tools to improve the yields of recombinant proteins which are difficult to produce in CHO cells. Biotechnol. Bioeng. 2016;113: 1094–1101. © 2015 Wiley Periodicals, Inc.