Literature DB >> 28876938

Lessons from the Hamster: Cricetulus griseus Tissue and CHO Cell Line Proteome Comparison.

Kelley M Heffner1, Deniz Baycin Hizal1, George S Yerganian2, Amit Kumar1, Özge Can3, Robert O'Meally4, Robert Cole4, Raghothama Chaerkady5, Herren Wu5, Michael A Bowen5, Michael J Betenbaugh1.   

Abstract

Chinese hamster ovary cells represent the dominant host for therapeutic recombinant protein production. However, few large-scale data sets have been generated to characterize this host organism and derived CHO cell lines at the proteomics level. Consequently, an extensive label-free quantitative proteomics analysis of two cell lines (CHO-S and CHO DG44) and two Chinese hamster tissues (liver and ovary) was used to identify a total of 11 801 unique proteins containing at least two unique peptides. 9359 unique proteins were identified specifically in the cell lines, representing a 56% increase over previous work. Additionally, 6663 unique proteins were identified across liver and ovary tissues, providing the first Chinese hamster tissue proteome. Protein expression was more conserved within cell lines during both growth phases than across cell lines, suggesting large genetic differences across cell lines. Overall, both gene ontology and KEGG pathway analysis revealed enrichment of cell-cycle activity in cells. In contrast, upregulated molecular functions in tissue include glycosylation and lipid transporter activity. Furthermore, cellular components including Golgi apparatus are upregulated in both tissues. In conclusion, this large-scale proteomics analysis enables us to delineate specific changes between tissues and cells derived from these tissues, which can help explain specific tissue function and the adaptations cells incur for applications in biopharmaceutical productions.

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Keywords:  CHO; KEGG; cell culture; gene ontology; hamster tissue; liver; mass spectrometry; ovary; pathway analysis; proteomics

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Year:  2017        PMID: 28876938     DOI: 10.1021/acs.jproteome.7b00382

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  4 in total

1.  Comparative systeomics to elucidate physiological differences between CHO and SP2/0 cell lines.

Authors:  Deniz Demirhan; Amit Kumar; Jie Zhu; Pi Camilla Poulsen; Natalia I Majewska; Yinong Sebastian; Raghothama Chaerkady; Wen Yu; Wei Zhu; Li Zhuang; Punit Shah; Kristen Lekstrom; Robert N Cole; Hui Zhang; Michael J Betenbaugh; Michael A Bowen
Journal:  Sci Rep       Date:  2022-02-28       Impact factor: 4.379

2.  Life at the periphery: what makes CHO cells survival talents.

Authors:  Tobias Jerabek; Florian Klingler; Nadja Raab; Nikolas Zeh; Jens Pfannstiel; Kerstin Otte
Journal:  Appl Microbiol Biotechnol       Date:  2022-08-30       Impact factor: 5.560

3.  A comprehensive CHO SWATH-MS spectral library for robust quantitative profiling of 10,000 proteins.

Authors:  Kae Hwan Sim; Lillian Chia-Yi Liu; Hwee Tong Tan; Kelly Tan; Daniel Ng; Wei Zhang; Yuansheng Yang; Stephen Tate; Xuezhi Bi
Journal:  Sci Data       Date:  2020-08-11       Impact factor: 6.444

4.  Expanded Chinese hamster organ and cell line proteomics profiling reveals tissue-specific functionalities.

Authors:  Kelley Heffner; Deniz Baycin Hizal; Natalia I Majewska; Swetha Kumar; Venkata Gayatri Dhara; Jie Zhu; Michael Bowen; Diane Hatton; George Yerganian; Athena Yerganian; Robert O'Meally; Robert Cole; Michael Betenbaugh
Journal:  Sci Rep       Date:  2020-09-28       Impact factor: 4.379

  4 in total

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