Literature DB >> 24081924

Model-directed engineering of "difficult-to-express" monoclonal antibody production by Chinese hamster ovary cells.

Leon P Pybus1, Greg Dean, Nathan R West, Andrew Smith, Olalekan Daramola, Ray Field, Stephen J Wilkinson, David C James.   

Abstract

Despite improvements in volumetric titer for monoclonal antibody (MAb) production processes using Chinese hamster ovary (CHO) cells, some "difficult-to-express" (DTE) MAbs inexplicably reach much lower process titers. These DTE MAbs require intensive cell line and process development activity, rendering them more costly or even unsuitable to manufacture. To rapidly and rationally identify an optimal strategy to improve production of DTE MAbs, we have developed an engineering design platform combining high-yielding transient production, empirical modeling of MAb synthesis incorporating an unfolded protein response (UPR) regulatory loop with directed expression and cell engineering approaches. Utilizing a panel of eight IgG1 λ MAbs varying >4-fold in volumetric titer, we showed that MAb-specific limitations on folding and assembly rate functioned to induce a proportionate UPR in host CHO cells with a corresponding reduction in cell growth rate. Derived from comparative empirical modeling of cellular constraints on the production of each MAb we employed two strategies to increase production of DTE MAbs designed to avoid UPR induction through an improvement in the rate/cellular capacity for MAb folding and assembly reactions. Firstly, we altered the transfected LC:HC gene ratio and secondly, we co-expressed a variety of molecular chaperones, foldases or UPR transactivators (BiP, CypB, PDI, and active forms of ATF6 and XBP1) with recombinant MAbs. DTE MAb production was significantly improved by both strategies, although the mode of action was dependent upon the approach employed. Increased LC:HC ratio or CypB co-expression improved cell growth with no effect on qP. In contrast, BiP, ATF6c and XBP1s co-expression increased qP and reduced cell growth. This study demonstrates that expression-engineering strategies to improve production of DTE proteins in mammalian cells should be product specific, and based on rapid predictive tools to assess the relative impact of different engineering interventions.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  Chinese hamster ovary cells; cell line engineering; difficult-to-express proteins; mathematical modeling; recombinant monoclonal antibody; unfolded protein response

Mesh:

Substances:

Year:  2013        PMID: 24081924     DOI: 10.1002/bit.25116

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  17 in total

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2.  Enhanced IgG1 production by overexpression of nuclear factor kappa B inhibitor zeta (NFKBIZ) in Chinese hamster ovary cells.

Authors:  Masayoshi Onitsuka; Yukie Kinoshita; Akitoshi Nishizawa; Tomomi Tsutsui; Takeshi Omasa
Journal:  Cytotechnology       Date:  2017-11-29       Impact factor: 2.058

3.  Systematic development of temperature shift strategies for Chinese hamster ovary cells based on short duration cultures and kinetic modeling.

Authors:  Jianlin Xu; Peifeng Tang; Andrew Yongky; Barry Drew; Michael C Borys; Shijie Liu; Zheng Jian Li
Journal:  MAbs       Date:  2018-10-02       Impact factor: 5.857

4.  Cleavage efficient 2A peptides for high level monoclonal antibody expression in CHO cells.

Authors:  Jake Chng; Tianhua Wang; Rui Nian; Ally Lau; Kong Meng Hoi; Steven C L Ho; Peter Gagnon; Xuezhi Bi; Yuansheng Yang
Journal:  MAbs       Date:  2015       Impact factor: 5.857

5.  Validation and identification of reference genes in Chinese hamster ovary cells for Fc-fusion protein production.

Authors:  Xiaonan Ma; Ling Zhang; Luming Zhang; Chenglong Wang; Xiaorui Guo; Yu Yang; Lin Wang; Xiangru Li; Ningning Ma
Journal:  Exp Biol Med (Maywood)       Date:  2020-03-26

6.  Multi-omic profiling -of EPO-producing Chinese hamster ovary cell panel reveals metabolic adaptation to heterologous protein production.

Authors:  Daniel Ley; Ali Kazemi Seresht; Mikael Engmark; Olivera Magdenoska; Kristian Fog Nielsen; Helene Faustrup Kildegaard; Mikael Rørdam Andersen
Journal:  Biotechnol Bioeng       Date:  2015-06-30       Impact factor: 4.530

7.  Mild hypothermia upregulates myc and xbp1s expression and improves anti-TNFα production in CHO cells.

Authors:  Mauro Torres; Roberto Zúñiga; Matias Gutierrez; Mauricio Vergara; Norberto Collazo; Juan Reyes; Julio Berrios; Juan Carlos Aguillon; Maria Carmen Molina; Claudia Altamirano
Journal:  PLoS One       Date:  2018-03-22       Impact factor: 3.240

Review 8.  Cell Line Techniques and Gene Editing Tools for Antibody Production: A Review.

Authors:  Arun K Dangi; Rajeshwari Sinha; Shailja Dwivedi; Sanjeev K Gupta; Pratyoosh Shukla
Journal:  Front Pharmacol       Date:  2018-06-12       Impact factor: 5.810

9.  Versatile microscale screening platform for improving recombinant protein productivity in Chinese hamster ovary cells.

Authors:  Henning Gram Hansen; Claes Nymand Nilsson; Anne Mathilde Lund; Stefan Kol; Lise Marie Grav; Magnus Lundqvist; Johan Rockberg; Gyun Min Lee; Mikael Rørdam Andersen; Helene Faustrup Kildegaard
Journal:  Sci Rep       Date:  2015-12-11       Impact factor: 4.379

10.  A protein chimera strategy supports production of a model "difficult-to-express" recombinant target.

Authors:  Hirra Hussain; David I Fisher; Robert G Roth; W Mark Abbott; Manuel Alejandro Carballo-Amador; Jim Warwicker; Alan J Dickson
Journal:  FEBS Lett       Date:  2018-07-03       Impact factor: 4.124

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