Batch‐to‐batch variability of two human designer cell lines – AGE1.HN and AGE1.HN.AAT – carried out by different laboratories under defined culture conditions using a mathematical model. Issue 6 (10th June 2013)

• Record Type: Journal Article
• Authors: Freund, Susann; Rath, Alexander; Barradas, Oscar Platas; Skerhutt, Eva; Scholz, Sebastian; Niklas, Jens; Sandig, Volker; Rose, Thomas; Heinzle, Elmar; Noll, Thomas; Pörtner, Ralf; Zeng, An Ping; Reichl, Udo
• Is Part Of: Engineering in life sciences. Volume 13:Issue 6(2013:Nov.)
• Page Start: 580
• Page End: 592
• Publication Date: 2013-06-10
• Subjects: Bioengineering -- Periodicals; 660.605
• DOI: 10.1002/elsc.201200111
• Languages: English
• ISSNs: 1618-0240

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Systems biology approaches involve collaboration of a larger number of research groups. Experiments are being performed in different laboratories dealing with different aspects of the topic of interest. Therefore, comparability of data collected for further analysis and modeling needs critical assessment. Here, growth and product formation of two human designer cell lines (AGE1.HN and its α1‐antitrypsin producing clone AGE1.HN.AAT) were investigated by four research laboratories. Cell lines were cultivated in shake flasks and stirred tank bioreactors operated at standardized conditions using a chemically defined medium, and a simple mathematical model was used to estimate characteristic process parameters. Results obtained for 35 batches showed that neither the initial viable cell concentration nor the initial concentration of glucose and glutamine showed significant differences between laboratories. For these measurements with low variations, specific growth rate and yields varied between 8.5 and 26% (relative standard error), indicating comparability of cultivations between laboratories for exponential growth. Higher variations of fitted parameters related to measurements with high initial variation. Comparing the nonproducing with the producing cell line, no significant differences were found regarding growth dynamics and metabolism. Overall, it seems justified to draw conclusions based on the entire experimental dataset of this systems biology project.</p> </abstract>