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在分批培养中,醋酸钠可提高表达ECD-Her1蛋白的HEK293细胞的生产力:实验结果与代谢通量分析。

Sodium acetate increases the productivity of HEK293 cells expressing the ECD-Her1 protein in batch cultures: experimental results and metabolic flux analysis.

作者信息

Pérez-Fernández Bárbara Ariane, Calzadilla Lisandra, Enrico Bena Chiara, Del Giudice Marco, Bosia Carla, Boggiano Tammy, Mulet Roberto

机构信息

Group of Complex Systems and Statistical Physics, Department of Applied Physics, Physics Faculty, University of Havana, Havana, Cuba.

Center of Molecular Immunology, Havana, Cuba.

出版信息

Front Bioeng Biotechnol. 2024 Apr 10;12:1335898. doi: 10.3389/fbioe.2024.1335898. eCollection 2024.

DOI:10.3389/fbioe.2024.1335898
PMID:38659646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11039900/
Abstract

Human Embryonic Kidney cells (HEK293) are a popular host for recombinant protein expression and production in the biotechnological industry. This has driven within both, the scientific and the engineering communities, the search for strategies to increase their protein productivity. The present work is inserted into this search exploring the impact of adding sodium acetate (NaAc) into a batch culture of HEK293 cells. We monitored, as a function of time, the cell density, many external metabolites, and the supernatant concentration of the heterologous extra-cellular domain ECD-Her1 protein, a protein used to produce a candidate prostate cancer vaccine. We observed that by adding different concentrations of NaAc (0, 4, 6 and 8 mM), the production of ECD-Her1 protein increases consistently with increasing concentration, whereas the carrying capacity of the medium decreases. To understand these results we exploited a combination of experimental and computational techniques. Metabolic Flux Analysis (MFA) was used to infer intracellular metabolic fluxes from the concentration of external metabolites. Moreover, we measured independently the extracellular acidification rate and oxygen consumption rate of the cells. Both approaches support the idea that the addition of NaAc to the culture has a significant impact on the metabolism of the HEK293 cells and that, if properly tuned, enhances the productivity of the heterologous ECD-Her1 protein.

摘要

人胚肾细胞(HEK293)是生物技术产业中重组蛋白表达和生产常用的宿主细胞。这促使科学界和工程界都在寻找提高其蛋白生产能力的策略。本研究即属于这一探索范畴,探究向HEK293细胞的分批培养物中添加醋酸钠(NaAc)的影响。我们监测了细胞密度、多种胞外代谢物以及用于生产候选前列腺癌疫苗的异源胞外结构域ECD-Her1蛋白的上清液浓度随时间的变化。我们观察到,通过添加不同浓度的NaAc(0、4、6和8 mM),ECD-Her1蛋白的产量随浓度增加而持续增加,而培养基的承载能力则下降。为理解这些结果,我们结合了实验和计算技术。代谢通量分析(MFA)用于从胞外代谢物浓度推断细胞内代谢通量。此外,我们还独立测量了细胞的胞外酸化率和耗氧率。这两种方法都支持这样一种观点,即向培养物中添加NaAc对HEK293细胞的代谢有显著影响,并且如果调节得当,可提高异源ECD-Her1蛋白的产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/0be09efea82e/fbioe-12-1335898-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/7fa5abc34421/fbioe-12-1335898-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/0fd0e94ce772/fbioe-12-1335898-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/6c6ee8f84151/fbioe-12-1335898-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/89d81350f4a6/fbioe-12-1335898-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/fb5b37151505/fbioe-12-1335898-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/d857013a94f4/fbioe-12-1335898-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/ae4d7578682b/fbioe-12-1335898-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/c52823c2597e/fbioe-12-1335898-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/0be09efea82e/fbioe-12-1335898-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/7fa5abc34421/fbioe-12-1335898-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/0fd0e94ce772/fbioe-12-1335898-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/6c6ee8f84151/fbioe-12-1335898-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/89d81350f4a6/fbioe-12-1335898-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/fb5b37151505/fbioe-12-1335898-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/d857013a94f4/fbioe-12-1335898-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/ae4d7578682b/fbioe-12-1335898-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/c52823c2597e/fbioe-12-1335898-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d1e/11039900/0be09efea82e/fbioe-12-1335898-g009.jpg

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