Cited by 54Viral Infectious Diseases and Gene Expression in InsectsProtein purification and stabilityMonoclonal and Polyclonal Antibodies Research

Identification of novel small molecule enhancers of protein production by cultured mammalian cells

Allen, Martin J., Boyce, James P., Trentalange, Michael T., Treiber, David L., Rasmussen, Brian, Tillotson, Benjamin, Davis, Raymond, Reddy, Pranhitha·2008·Biotechnology and Bioengineering

Abstract

Small molecule additives to cell culture media (e.g., sodium butyrate) that are capable of enhancing the expression of recombinant proteins have significant utility in the production and manufacture of therapeutic polypeptides. To identify novel small molecule enhancers (SMEs) of recombinant protein expression in Chinese Hamster Ovary (CHO) cells, we screened two separate small molecule libraries for compounds capable of enhancing the expression of either a fluorescent reporter protein or a monoclonal antibody. Several compounds that increased recombinant protein expression were identified, and these compounds fell into three broad classes: (1) aromatic carboxylic acids, (2) hydroxamic acids, and (3) acetamides. We examined the impact of SME addition to CHO cell cultures expressing different classes of recombinant proteins including monoclonal antibodies (MAbs). For CHO cell pools or clones grown in production shake‐flasks or bioreactors, recombinant protein titers up to 60% higher than control cultures were observed. Analysis of mRNA levels suggest that transcriptional activation plays a role in the expression enhancement seen for some SMEs, but other mechanisms may be involved for at least one compound. Finally, we tested many of the identified SMEs for their ability to increase MAb production by a hybridoma cell line. Hexanohydroxamic acid increased shake‐flask MAb production by 40% relative to a control. Taken together, these data demonstrate the potential utility of the compounds in the production of therapeutically relevant proteins from diverse cell‐based production systems. Biotechnol. Bioeng. 2008;100: 1193–1204. © 2008 Wiley Periodicals, Inc.

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Crossref · 10.1002/bit.21839

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  • Numerous small molecules have been identified from a chemical library that could enhance protein production.

    “Beside media and feeds, numerous small molecules have been identified from a chemical library that could enhance protein production (Allen et al., 2008).”

    From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Allen et al., 2008

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Authors
Allen, M. J., Boyce, J. P., Trentalange, M. T., Treiber, D. L., Rasmussen, B., Tillotson, B., Davis, R., & Reddy, P.
Affiliations
Amgen (United States) (US)
Corresponding author
Allen, Martin J.
Venue
Biotechnology and Bioengineering
Publisher
Wiley
Published
2008-03-19
Volume
100
Issue
6
Pages
1193-1204
ISSN
  • 0006-3592 (ISSN-L)
  • 1097-0290
OpenAlex
W2026058196
Cited by
54
References
0
Citations by year
2026: 1 · 2025: 1 · 2024: 3 · 2023: 1 · 2022: 2 · 2021: 3 · 2020: 5 · 2019: 2 · 2018: 2 · 2017: 8 · 2016: 3 · 2015: 4 · 2014: 2 · 2013: 4 · 2012: 1
FWCI
1.64
Type
journal article
Language
en
Open access
closed
Locations
  • Biotechnology and Bioengineering (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
Keywords
small molecule enhancers, recombinant protein expression, CHO cells, monoclonal antibody production, hybridoma, hydroxamic acids, aromatic carboxylic acids, acetamide, transcriptional activation, bioreactor production
MeSH terms
Acetamides, Animals, Antibodies, Monoclonal, Caproates, Cricetulus, Culture Media, Female, Fluorescent Dyes, Cricetinae, Hybridomas, Hydrocarbons, Aromatic, Hydroxamic Acids, Recombinant Fusion Proteins, Transcriptional Activation, Gene Expression, CHO Cells, Cell Culture Techniques, Bioreactors, Genetic Enhancement

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