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The emerging role of systems biology for engineering protein production in CHO cells

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CURRENT OPINION IN BIOTECHNOLOGY
卷 51, 期 -, 页码 64-69

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CURRENT BIOLOGY LTD
DOI: 10.1016/j.copbio.2017.11.015

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资金

  1. Novo Nordisk Foundation [NNF1OCC1016517]
  2. NIGIVIS [R35 GM119850]
  3. Government of Mexico (CONACYT)
  4. University of California Institute for Mexico
  5. United States (UC-MEXUS)
  6. Taiwan Ministry of Education
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R35GM119850, T32GM008806] Funding Source: NIH RePORTER
  8. Novo Nordisk Fonden [NNF10CC1016517] Funding Source: researchfish
  9. NNF Center for Biosustainability [CHO in Silico Protein Quality Engin] Funding Source: researchfish

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To meet the ever-growing demand for effective, safe, and affordable protein therapeutics, decades of intense efforts have aimed to maximize the quantity and quality of recombinant proteins produced in CHO cells. Bioprocessing innovations and cell engineering efforts have improved product titer; however, uncharacterized cellular processes and gene regulatory mechanisms still hinder cell growth, specific productivity, and protein quality. Herein, we summarize recent advances in systems biology and data-driven approaches aiming to unravel how molecular pathways, cellular processes, and extrinsic factors (e.g. media supplementation) influence recombinant protein production. In particular, as the available omics data for CHO cells continue to grow, predictive models and screens will be increasingly used to unravel the biological drivers of protein production, which can be used with emerging genome editing technologies to rationally engineer cells to further control the quantity, quality and affordability of many biologic drugs.

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