Cited by 137Virus-based gene therapy researchAnimal Genetics and ReproductionViral Infectious Diseases and Gene Expression in Insects

A mammalian artificial chromosome engineering system (ACE System) applicable to biopharmaceutical protein production, transgenesis and gene-based cell therapy

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Lindenbaum, Michael, Perkins, Ed, Csonka, Erika, Fleming, Elena, Garcia, Lisa, Greene, Amy, Gung, Lindsay, Hadlaczky, Gyula +13 more·2004·Nucleic Acids Research

Abstract

Mammalian artificial chromosomes (MACs) provide a means to introduce large payloads of genetic information into the cell in an autonomously replicating, non-integrating format. Unique among MACs, the mammalian satellite DNA-based Artificial Chromosome Expression (ACE) can be reproducibly generated de novo in cell lines of different species and readily purified from the host cells' chromosomes. Purified mammalian ACEs can then be re-introduced into a variety of recipient cell lines where they have been stably maintained for extended periods in the absence of selective pressure. In order to extend the utility of ACEs, we have established the ACE System, a versatile and flexible platform for the reliable engineering of ACEs. The ACE System includes a Platform ACE, containing >50 recombination acceptor sites, that can carry single or multiple copies of genes of interest using specially designed targeting vectors (ATV) and a site-specific integrase (ACE Integrase). Using this approach, specific loading of one or two gene targets has been achieved in LMTK(-) and CHO cells. The use of the ACE System for biological engineering of eukaryotic cells, including mammalian cells, with applications in biopharmaceutical production, transgenesis and gene-based cell therapy is discussed.

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Crossref · 10.1093/nar/gnh169

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  • ACE technology was shown to be effective for establishing CHO cell lines producing respectable titers of monoclonal antibody.

    “It was shown to be effective for establishing CHO cell lines producing respectable titers of monoclonal antibody (Lindenbaum et al., 2004;Kennard et al., 2009;Kennard 2011).”

    From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Lindenbaum et al., 2004

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Authors
Lindenbaum, M., Perkins, E., Csonka, E., Fleming, E., Garcia, L., Greene, A., Gung, L., Hadlaczky, G., Lee, E., Leung, J., MacDonald, N., Maxwell, A., Mills, K., Monteith, D., Perez, C. F., Shellard, J., Stewart, S., Stodola, T., Vandenborre, D., Vanderbyl, S., & Ledebur, H. C.
Corresponding author
Lindenbaum, Michael
Venue
Nucleic Acids Research
Published
2004
Volume
32
Issue
21
Pages
e172-e172
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2097496703
Cited by
137
References
0
Citations by year
2022: 1 · 2021: 6 · 2020: 4 · 2019: 5 · 2018: 4 · 2017: 6 · 2016: 2 · 2015: 6 · 2014: 9 · 2013: 10 · 2012: 9
FWCI
6.96
Type
journal article
Language
en
Open access
Locations
  • Nucleic Acids Research (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
Institute of Materials Research and Engineering
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Animal Genetics and Reproduction
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
Keywords
satellite DNA, targeting vector, transgenesis, CHO cells
MeSH terms
Animals, Cell Line, Cricetulus, Drug Industry, Erythropoietin, Genetic Engineering, Cricetinae, Humans, Recombinant Proteins, Genetic Therapy, CHO Cells, Mice, SCID, Mice, Inbred NOD, Integrases, Chromosomes, Artificial, Mammalian, Animals, Genetically Modified, Mice

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