바이오 교육훈련을 위한 Rituximab 발현 재조합 CHO 세포주의 특성 분석
Characterization of Recombinant Rituximab-Producing CHO Cells for Biotechnical Education and Training
0
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
In this study, we investigated the growth and production characteristics of a Recombinant rituximab-producing CHO cell line in an economic, serum-free medium. The cell line showed a typical cell growth curve with high viability in a 25 mL Erlenmeyer flask suspension culture. The maximum expression level of Rituximab was 224.3 mg/L, which increased in proportional to the number of viable cells over the culture time. SDS-PAGE analysis under non-reducing and reducing conditions showed that the recombinant cell line secreted Rituximab with a predicted molecular weight, having the proper heavy and light chains. In addition, the production level was high enough to be detected on the SDS-PAGE by Coomassie staining. To investigate the feasibility of the cell culture supernatant as a component of biocosmetic products, both a cream formulation containing the cell culture supernatant and a serum-free control medium were prepared. without any visible disturbance, so that this recipe could be utilized for biocosmetic experiment education. Taken together, this study suggests that the presented recombinant CHO cell line could be a useful experimental tool in bioprocess and biocosmetic technology education and training.
Abstract
In this study, we investigated the growth and production characteristics of a Recombinant rituximab-producing CHO cell line in an economic, serum-free medium. The cell line showed a typical cell growth curve with high viability in a 25 mL Erlenmeyer flask suspension culture. The maximum expression level of Rituximab was 224.3 mg/L, which increased in proportional to the number of viable cells over the culture time. SDS-PAGE analysis under non-reducing and reducing conditions showed that the recombinant cell line secreted Rituximab with a predicted molecular weight, having the proper heavy and light chains. In addition, the production level was high enough to be detected on the SDS-PAGE by Coomassie staining. To investigate the feasibility of the cell culture supernatant as a component of biocosmetic products, both a cream formulation containing the cell culture supernatant and a serum-free control medium were prepared. without any visible disturbance, so that this recipe could be utilized for biocosmetic experiment education. Taken together, this study suggests that the presented recombinant CHO cell line could be a useful experimental tool in bioprocess and biocosmetic technology education and training.
참고문헌 (11)
- Li Feng, "Cell culture process for monoclonal antibody production", mAb, 2(5), pp.466~479 (2010)
- BioRN, "Cell culture technology: hamster cells and the production of biopharmaceuticals" (2011), BIOPRO Baden-Württemberg GmbH
- Hunter, M., "Optimization of protein expression in mammalian cells", Current Protocols in Protein Science, 95, pp.1~28 (2018)
- Singh, S.K., "Structural and functional comparability study of anti-CD20 monoclonal antibody with reference product2", Biologics, 12, pp.159~170 (2018)
- 이유순, "미생물 복합발효 배양물의 피부 적용성과 화장품 개발", 한국식품영양과학회한국식품영양과학회 학술대회발표집, 10, pp.316~ (2007)
- 최은주, "인간 피부줄기세포 배지의 개발과 이를 조성물로 제조한 화장품의 유효성 평가", 아시안뷰티화장품학술지, 10(4), pp.949~960 (2012), 한국피부과학연구원
- Park, J. H., "Proteomic analysis of host cell protein dynamics in the culture supernatants of antibody-producing CHO cells", Scientific Reports, 7(44246), pp.1~13 (2017)
- Noh, S. M., "Comprehensive characterization of glutamine synthetasemediated selection for the establishment of recombinant CHO cells producing monoclonal antibodies", Scientific Reports, 8(5361), pp.1~11 (2018)
- Schindelin, J., "The ImageJ ecosystem: An open platform for biomedical image analysis", Molecular Reproduction and Development, PMID, 2615~3368 (2015)
- Renad, J.M., "Evidence that monoclonal antibody production kinetics is related to the integral of viable cells curve in batch systems", Biotechnol. Lett., 10(2), pp.91~96 (1988)
- Lee, G. M., "Production of monoclonal antibody using freesuspended and immobilized hybridoma cells: effects of serum", Biotechnol. Bioeng., 38, pp.821~830 (1991)
