Literature DB >> 23335490

A CHO cell line engineered to express XBP1 and ERO1-Lα has increased levels of transient protein expression.

Katharine Cain1, Shirley Peters, Hanna Hailu, Bernie Sweeney, Paul Stephens, James Heads, Kaushik Sarkar, Andy Ventom, Catherine Page, Alan Dickson.   

Abstract

Transient gene expression (TGE) systems currently provide rapid and scalable (up to 100 L) methods for generating multigram quantities of recombinant heterologous proteins. Product titers of up to 1 g/L have been demonstrated in HEK293 cells but reported yields from Chinese hamster ovary (CHO) cells are lower at ∼300 mg/L. We report on the establishment of an engineered CHOS cell line, which has been developed for TGE. This cell line has been engineered to express both X-box binding protein (XBP-1S) and endoplasmic reticulum oxidoreductase (ERO1-Lα) and has been named CHOS-XE. CHOS-XE cells produced increased antibody (MAb) yields (5.3- 6.2 fold) in comparison to CHOS cells. Product quality was unchanged as assessed by size, charge, propensity to aggregate, major glycosylation species, and thermal stability. To further develop and test this TGE system, five commercial media were assessed, and one was shown to offer the greatest increase in antibody yields. With the addition of a commercial feed, MAb titers reached 875 mg/L.
© 2013 American Institute of Chemical Engineers.

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Year:  2013        PMID: 23335490     DOI: 10.1002/btpr.1693

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  20 in total

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2.  Development of Genetically Modified Chinese Hamster Ovary Host Cells for the Enhancement of Recombinant Tissue Plasminogen Activator Expression.

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Review 3.  N-Glycan-based ER Molecular Chaperone and Protein Quality Control System: The Calnexin Binding Cycle.

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Journal:  Traffic       Date:  2016-01-10       Impact factor: 6.215

4.  CHO-S antibody titers >1 gram/liter using flow electroporation-mediated transient gene expression followed by rapid migration to high-yield stable cell lines.

Authors:  Krista Steger; James Brady; Weili Wang; Meg Duskin; Karen Donato; Madhusudan Peshwa
Journal:  J Biomol Screen       Date:  2014-12-17

5.  Development of a fluorescent reporter system for monitoring ER stress in Chinese hamster ovary cells and its application for therapeutic protein production.

Authors:  Gargi Roy; Shu Zhang; Lina Li; Eileen Higham; Herren Wu; Marcello Marelli; Michael A Bowen
Journal:  PLoS One       Date:  2017-08-23       Impact factor: 3.240

6.  Exploring cellular behavior under transient gene expression and its impact on mAb productivity and Fc-glycosylation.

Authors:  Si N Sou; Ken Lee; Kalpana Nayyar; Karen M Polizzi; Christopher Sellick; Cleo Kontoravdi
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7.  Fab-dsFv: A bispecific antibody format with extended serum half-life through albumin binding.

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Journal:  MAbs       Date:  2016-08-17       Impact factor: 5.857

8.  Using molecular markers to characterize productivity in Chinese hamster ovary cell lines.

Authors:  Raihana Z Edros; Susan McDonnell; Mohamed Al-Rubeai
Journal:  PLoS One       Date:  2013-10-17       Impact factor: 3.240

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.  Extending the half-life of a fab fragment through generation of a humanized anti-human serum albumin Fv domain: An investigation into the correlation between affinity and serum half-life.

Authors:  Ralph Adams; Laura Griffin; Joanne E Compson; Mark Jairaj; Terry Baker; Tom Ceska; Shauna West; Oliver Zaccheo; Emma Davé; Alastair Dg Lawson; David P Humphreys; Sam Heywood
Journal:  MAbs       Date:  2016-06-17       Impact factor: 5.857

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