A feed enrichment strategy targeting the tricarboxylic acid cycle for increasing monoclonal antibody production and alleviating ammonia accumulation in Chinese hamster ovary cell culture

被引:4
作者
Saldanha, Marianne [1 ]
Padhye, Krutika [1 ,2 ]
Warke, Vishal G. [3 ]
Dandekar, Prajakta [4 ]
Jain, Ratnesh [1 ]
机构
[1] Inst Chem Technol, Dept Biol Sci & Biotechnol, Mumbai 400019, India
[2] Spinco Biotech Pvt Ltd, Shree Nand Dham, Sect 11 CBD Belapur, Navi Mumbai 400614, India
[3] MIDC, Himedia Labs Pvt Ltd, Plot C40, Thane West 400604, India
[4] Inst Chem Technol, Dept Pharmaceut Sci & Technol, Mumbai 400019, India
关键词
Chinese hamster ovary cells; Monoclonal antibody; Tricarboxylic acid cycle; Critical quality attributes; Feed development; Feed enrichment; CHO-CELLS; SUBSTITUTION; GLUTAMINE;
D O I
10.1016/j.bej.2023.108836
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study, we demonstrated a simple strategy for increasing mAb production by enriching an existing feed with TCA cycle intermediates and precursors. TCA cycle intermediates/precursors were tested individually and as mixtures, termed as 'Enriched Feeds'. The enriched feed mixtures were tested in two compositions comprising: (i) only TCA intermediates/precursors that individually increased mAb titre (EF_Partial) and, (ii) all TCA in-termediates/precursors (EF_Complete). These mixtures were also tested for initiation at two phases: (i) from Day 3 (start of exponential phase) and, (ii) from Day 6 (start of stationary phase), and at two concentration levels (high and low). Our results showed that the EF_Partial mixtures were more efficient in increasing mAb titre as compared to the EF_Complete mixtures. The EF_Partial_D6_Low mixture gave the highest titre increase of 55 %, as compared to the control culture. Additionally, a decrease in ammonia production was observed immediately upon the supply of the enriched feeds. In the individual assessment, succinate supplementation resulted in a superior cell growth profile and also exhibited the most significant reduction in ammonia. The individually tested TCA compounds and mixtures also did not impact mAb quality. Therefore, in this study, we demonstrate that a simple approach of enriching feeds with TCA cycle intermediates/precursors effectively increases mAb pro-duction by > 50 % without affecting quality attributes.
引用
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页数:11
相关论文
共 24 条
  • [1] Towards dynamic metabolic flux analysis in CHO cell cultures
    Ahn, Woo Suk
    Antoniewicz, Maciek R.
    [J]. BIOTECHNOLOGY JOURNAL, 2012, 7 (01) : 61 - 74
  • [2] Bender D.A, 2003, ENCY FOOD SCI NUTR, P5851, DOI [10.1016/B0-12-227055-X/01363-8, DOI 10.1016/B0-12-227055-X/01363-8]
  • [3] Bonarius HPJ, 1998, BIOTECHNOL BIOENG, V57, P447, DOI 10.1002/(SICI)1097-0290(19980220)57:4<447::AID-BIT8>3.3.CO
  • [4] 2-C
  • [5] Metabolomics profiling of extracellular metabolites in recombinant Chinese Hamster Ovary fed-batch culture
    Chong, William P. K.
    Goh, Lin Tang
    Reddy, Satty G.
    Yusufi, Faraaz N. K.
    Lee, Dong Yup
    Wong, Niki S. C.
    Heng, Chew Kiat
    Yap, Miranda G. S.
    Ho, Ying Swan
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2009, 23 (23) : 3763 - 3771
  • [6] Metabolic Profiling of CHO Cells during the Production of Biotherapeutics
    Coulet, Mathilde
    Kepp, Oliver
    Kroemer, Guido
    Basmaciogullari, Stephane
    [J]. CELLS, 2022, 11 (12)
  • [7] Metabolic analysis of antibody producing CHO cells in fed-batch production
    Dean, Jason
    Reddy, Pranhitha
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2013, 110 (06) : 1735 - 1747
  • [8] Engelking L.R., 2015, Textbook of Veterinary Physiological Chemistry, P214, DOI [10.1016/B978-0-12-391909-0.50035-9, DOI 10.1016/B978-0-12-391909-0.50035-9]
  • [9] CATABOLIC CONTROL OF MAMMALIAN-CELL CULTURE
    GLACKEN, MW
    [J]. BIO-TECHNOLOGY, 1988, 6 (09): : 1041 - &
  • [10] Effect of glutamine substitution by TCA cycle intermediates on the production and sialylation of Fc-fusion protein in Chinese hamster ovary cell culture
    Ha, Tae Kwang
    Lee, Gyun Min
    [J]. JOURNAL OF BIOTECHNOLOGY, 2014, 180 : 23 - 29