Title of article :
Quantitative Proteomic Analysis of Cellular Responses to a Designed Amino Acid Feed in a Monoclonal Antibody Producing Chinese Hamster Ovary Cell Line
Author/Authors :
Torkashvand, Fatemeh Medical Biotechnology Department - Biotechnology Research Center - Pasteur Institute of Iran, Tehran, Iran , Mahboudi, Fereidoun Medical Biotechnology Department - Biotechnology Research Center - Pasteur Institute of Iran, Tehran, Iran , Vossoughi, Manouchehr Department of Chemical and Petroleum Engineering - Biochemical and Bioenvironmental Research Center Sharif University of Technology, Tehran, Iran , Fatemi, Elnaz Medical Biotechnology Department - Biotechnology Research Center - Pasteur Institute of Iran, Tehran, Iran , Moosavi Basri, Masoud Medical Biotechnology Department - Biotechnology Research Center - Pasteur Institute of Iran, Tehran, Iran , Heydari, Amir Department of Chemical Engineering - University of Mohaghegh Ardabili, Ardabil, Iran , Vaziri, Behrouz Medical Biotechnology Department - Biotechnology Research Center - Pasteur Institute of Iran, Tehran, Iran
Pages :
9
From page :
385
To page :
393
Abstract :
Background: Chinese hamster ovary (CHO) cell line is considered as the most common cell line in the biopharmaceutical industry because of its capability in performing efficient post-translational modifications and producing the recombinant proteins, which are similar to natural human proteins. The optimization of the upstream process via different feed strategies has a great impact on the target molecule expression and yield. Methods: To determine and understand the molecular events beneath the feed effects on the CHO cell, a labelfree quantitative proteomic analysis was applied. The proteome changes followed by the addition of a designed amino acid feed to the monoclonal antibody producing CHO cell line culture medium were investigated. Results: The glutathione synthesis, the negative regulation of the programmed cell death, proteasomal catabolic process, and the endosomal transport pathway were up-regulated in the group fed with a designed amino acid feed compared to the control group. Conclusion: Our findings could be helpful to identify new targets for metabolic engineering.
Keywords :
Proteomics , Monoclonal antibodies , Glutathione , CHO cells
Journal title :
Astroparticle Physics
Serial Year :
2018
Record number :
2482250
Link To Document :
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