Literature DB >> 29150912

Sustaining an efficient and effective CHO cell line development platform by incorporation of 24-deep well plate screening and multivariate analysis.

Alessandro Mora1,2, Sheng Sam Zhang1, Gerald Carson1, Bernard Nabiswa1, Patrick Hossler3, Seongkyu Yoon2.   

Abstract

Efficient and effective cell line screening is paramount toward a successful biomanufacturing program. Here we describe the implementation of 24-deep well plate (24-DWP) screening of CHO lines as part of the cell line development platform at AbbVie. Incorporation of this approach accelerated the identification of the best candidate lines for process development. In an effort to quantify and predict process performance comparability, we compared cell culture performance in and in shake flasks, for a panel of Chinese Hamster Ovary cell lines expressing a monoclonal antibody. The results in 24-DWP screening showed reduced growth profiles, but comparable viability profiles. Slow growers in 24-DWP achieved the highest productivity improvement upon scaling-up to shake flasks. Product quality of the protein purified from shake flasks and 24-DWP were also compared. The 24-DWP culture conditions were found to influence the levels of acidic species, reduce the G0 N-glycan species, and increase the high-mannose N-glycan species. Nevertheless, the identification of undesirable profiles is executed consistently with the scaled-up culture. We further employed multivariate data analysis to capture differences depending on the two scales and we could demonstrate that cell line profiles were adequately clustered, regardless of the vessel used for the development. In conclusion, the 24-DWP platform was reasonably predictive of the parameters crucial for upstream process development activities, and has been adapted as part of the AbbVie cell line development platform.
© 2017 American Institute of Chemical Engineers Biotechnol. Prog., 34:175-186, 2018. © 2017 American Institute of Chemical Engineers.

Entities:  

Keywords:  24-deep well plate; Chinese Hamster Ovary; cell culture; cell line development; scale-down

Mesh:

Substances:

Year:  2017        PMID: 29150912     DOI: 10.1002/btpr.2584

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


  4 in total

1.  Early integration of Design of Experiment (DOE) and multivariate statistics identifies feeding regimens suitable for CHO cell line development and screening.

Authors:  Alessandro Mora; Bernard Nabiswa; Yuanyuan Duan; Sheng Zhang; Gerald Carson; Seongkyu Yoon
Journal:  Cytotechnology       Date:  2019-11-09       Impact factor: 2.058

2.  Microfluidic chip-based single-cell cloning to accelerate biologic production timelines.

Authors:  Jonathan Diep; Huong Le; Kim Le; Ewelina Zasadzinska; Jasmine Tat; Pheng Yam; Ryan Zastrow; Natalia Gomez; Jennitte Stevens
Journal:  Biotechnol Prog       Date:  2021-08-10

3.  Screening and selection strategy for the establishment of biosimilar to trastuzumab-expressing CHO-K1 cell lines.

Authors:  Thailin Lao-Gonzalez; Alexi Bueno-Soler; Arnelys Duran-Hernandez; Katya Sosa-Aguiar; Luis Eduardo Hinojosa-Puerta; Tays Hernandez-Garcia; Kathya Rashida de la Luz-Hernandez; Julio Palacios-Oliva; Tammy Boggiano-Ayo
Journal:  AMB Express       Date:  2021-01-03       Impact factor: 3.298

4.  Online 2D Fluorescence Monitoring in Microtiter Plates Allows Prediction of Cultivation Parameters and Considerable Reduction in Sampling Efforts for Parallel Cultivations of Hansenula polymorpha.

Authors:  Christoph Berg; Nina Ihling; Maurice Finger; Olivier Paquet-Durand; Bernd Hitzmann; Jochen Büchs
Journal:  Bioengineering (Basel)       Date:  2022-09-04
  4 in total

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