Development and characterization of an automated imaging workflow to generate clonally-derived cell lines for therapeutic proteins

Biotechnol Prog. 2018 May;34(3):584-592. doi: 10.1002/btpr.2561. Epub 2017 Oct 10.

Abstract

In the development of biopharmaceutical products, the expectation of regulatory agencies is that the recombinant proteins are produced from a cell line derived from a single progenitor cell. A single limiting dilution step followed by direct imaging, as supplemental information, provides direct evidence that a cell line originated from a single progenitor cell. To obtain this evidence, a high-throughput automated imaging system was developed and characterized to consistently ensure that cell lines used for therapeutic protein production are clonally-derived. Fluorescent cell mixing studies determined that the automated imaging workflow and analysis provide ∼95% confidence in accurately and precisely identifying one cell in a well. Manual inspection of the images increases the confidence that the cell line was derived from a single-cell to >99.9%. © 2017 American Institute of Chemical Engineers Biotechnol. Prog., 34:584-592, 2018.

Keywords: automated high-throughput imaging; cell line development; clonally-derived cell line; single-cell cloning.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / biosynthesis*
  • Antibodies, Monoclonal / therapeutic use
  • Automation*
  • CHO Cells
  • Cell Culture Techniques*
  • Clone Cells / cytology*
  • Clone Cells / metabolism*
  • Cricetulus
  • High-Throughput Screening Assays
  • Image Processing, Computer-Assisted*
  • Recombinant Proteins / biosynthesis*
  • Recombinant Proteins / therapeutic use

Substances

  • Antibodies, Monoclonal
  • Recombinant Proteins