Proteomic analysis of host cell protein dynamics in the supernatant of Fc‐fusion protein‐producing CHO DG44 and DUKX‐B11 cell lines in batch and fed‐batch cultures. Issue 10 (11th July 2017)
- Record Type:
- Journal Article
- Title:
- Proteomic analysis of host cell protein dynamics in the supernatant of Fc‐fusion protein‐producing CHO DG44 and DUKX‐B11 cell lines in batch and fed‐batch cultures. Issue 10 (11th July 2017)
- Main Title:
- Proteomic analysis of host cell protein dynamics in the supernatant of Fc‐fusion protein‐producing CHO DG44 and DUKX‐B11 cell lines in batch and fed‐batch cultures
- Authors:
- Park, Jin Hyoung
Jin, Jong Hwa
Ji, In Jung
An, Hyun Joo
Kim, Jong Won
Lee, Gyun Min - Abstract:
- ABSTRACT: Chinese hamster ovary (CHO) cells are the most widely used host cell lines for the commercial production of therapeutic proteins including Fc‐fusion proteins. During the culture of recombinant CHO (rCHO) cells, host cell proteins (HCPs), secreted from viable cells and released from dead cells, accumulate extracellularly, potentially impairing product quality. In this study, the HCPs that accumulated extracellularly in batch and fed‐batch cultures of Fc‐fusion protein‐producing rCHO cell lines (DG‐Fc and DUKX‐Fc) were identified and quantified using nanoflow liquid chromatography–tandem mass spectrometry (LC–MS/MS), followed by gene ontology and functional analysis. When the proteome database of Cricetulus griseus was used as a reference to identify the HCPs, more HCPs were identified for DG‐Fc (1632 HCPs in batch culture and 1733 HCPs in fed‐batch culture) than for DUKX‐Fc (1114 HCPs in batch culture and 1002 HCPs in fed‐batch culture). Clustering analysis of HCPs, which were classified into four clusters according to their concentration profiles during culture, showed that the concentration profiles of HCPs affecting the quality of Fc‐fusion proteins correlated with changes in Fc‐fusion protein quality. Taken together, the dataset of HCPs obtained in this study using the two different rCHO cell lines provides insights into the determination of appropriate target proteins to be removed during the culture and purification steps so as to ensure good Fc‐fusion proteinABSTRACT: Chinese hamster ovary (CHO) cells are the most widely used host cell lines for the commercial production of therapeutic proteins including Fc‐fusion proteins. During the culture of recombinant CHO (rCHO) cells, host cell proteins (HCPs), secreted from viable cells and released from dead cells, accumulate extracellularly, potentially impairing product quality. In this study, the HCPs that accumulated extracellularly in batch and fed‐batch cultures of Fc‐fusion protein‐producing rCHO cell lines (DG‐Fc and DUKX‐Fc) were identified and quantified using nanoflow liquid chromatography–tandem mass spectrometry (LC–MS/MS), followed by gene ontology and functional analysis. When the proteome database of Cricetulus griseus was used as a reference to identify the HCPs, more HCPs were identified for DG‐Fc (1632 HCPs in batch culture and 1733 HCPs in fed‐batch culture) than for DUKX‐Fc (1114 HCPs in batch culture and 1002 HCPs in fed‐batch culture). Clustering analysis of HCPs, which were classified into four clusters according to their concentration profiles during culture, showed that the concentration profiles of HCPs affecting the quality of Fc‐fusion proteins correlated with changes in Fc‐fusion protein quality. Taken together, the dataset of HCPs obtained in this study using the two different rCHO cell lines provides insights into the determination of appropriate target proteins to be removed during the culture and purification steps so as to ensure good Fc‐fusion protein quality. Biotechnol. Bioeng. 2017;114: 2267–2278. © 2017 Wiley Periodicals, Inc. Abstract : During the culture of recombinant CHO (rCHO) cells, host cell proteins (HCPs), secreted from viable cells and released from dead cells, accumulate extracellularly, potentially impairing product quality. The HCPs that accumulated extracellularly in batch and fed‐batch cultures of rCHO cell lines were identified and quantified using LC‐MS/MS. The dataset of HCPs obtained in this study provides insights towards establishing effective methods to ensure high quality and stability of Fc‐fusion proteins in rCHO cell cultures. … (more)
- Is Part Of:
- Biotechnology and bioengineering. Volume 114:Issue 10(2017)
- Journal:
- Biotechnology and bioengineering
- Issue:
- Volume 114:Issue 10(2017)
- Issue Display:
- Volume 114, Issue 10 (2017)
- Year:
- 2017
- Volume:
- 114
- Issue:
- 10
- Issue Sort Value:
- 2017-0114-0010-0000
- Page Start:
- 2267
- Page End:
- 2278
- Publication Date:
- 2017-07-11
- Subjects:
- host cell proteins -- Chinese hamster ovary cells -- proteomics -- Fc‐fusion protein -- product quality -- fed‐batch culture
Biotechnology -- Periodicals
Bioengineering -- Periodicals
660.6 - Journal URLs:
- http://onlinelibrary.wiley.com/doi/10.1002/bip.v101.5/issuetoc ↗
http://www.interscience.wiley.com ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/bit.26360 ↗
- Languages:
- English
- ISSNs:
- 0006-3592
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10518.xml