Advancement in recombinant protein production using a marine oxygen carrier to enhance oxygen transfer in a CHO-S cell line

被引:15
作者
Le Pape, Fiona [1 ,2 ]
Bossard, Morgane [2 ]
Dutheil, Delphine [2 ]
Rousselot, Morgane [2 ]
Polard, Valerie [2 ]
Ferec, Claude [1 ,4 ,5 ]
Leize, Elisabeth [1 ,3 ]
Delepine, Pascal [1 ,5 ]
Zal, Franck [2 ]
机构
[1] European Brittany Univ, Univ Western Brittany, Funct Genet Dept, INSERM,Res Unit 1078, F-29218 Brest 02, France
[2] HEMARINA SA, Aeropole Ctr, F-29600 Morlaix, France
[3] Reg Univ Hosp Ctr Brest, Protesis Dept, Res & Format Unit Odontol, F-29238 Brest, France
[4] Reg Univ Hosp Ctr Brest, Funct Genet Dept, F-29238 Brest, France
[5] French Blood Serv Brittany, F-29218 Brest 02, France
关键词
bioprocessing; cell growth rate; cell viability; CHO-S cells; CHO shear stress; marine oxygen additive; Oxygen carrier; oxygen transfer rate; recombinant-protein; HAMSTER OVARY CELLS; EXTRACELLULAR HEMOGLOBIN; MONOCLONAL-ANTIBODY; MAMMALIAN-CELLS; APOPTOSIS INHIBITION; ARENICOLA-MARINA; BATCH CULTURES; GROWTH; THERAPEUTICS; SURVIVAL;
D O I
10.3109/21691401.2015.1029632
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
Recombinant proteins, particularly proteins used as therapeutics, are widely expressed for bioprocessing manufacturing processes. Mammalian cell lines represent the major host cells for bioproduction, according to their capacities of post-translational modifications and folding of secreted proteins. Many parameters can affect cell productivity, especially the rate of oxygen transfer. Dissolved oxygen, in high or low proportions, is a crucial parameter which can affect cell viability and thus productivity. HEMARINA has developed a new technology, commercially proposed as HEMOXCell (R), to improve cell culture at a large production scale. HEMOXCell (R) is a marine oxygen carrier having properties of high oxygen sensitivity, to be used as an oxygen additive during cell culture manufacturing. In this study, we investigated the effects of HEMOXCell (R) on the culture of the commonly used CHO-S cell line. Two main objectives were pursued: 1) cell growth rate and viability during a batch mode process, and 2) the determination of the effect of this oxygen carrier on recombinant protein production from a CHO-transfected cell line. Our results show an increase of CHO-S cellular growth at a rate of more than four-fold in culture with HEMOXCell (R). Moreover, an extension of the growth exponential phase and high cell viability were observed. All of these benefits seem to contribute to the improvement of recombinant protein production. This work underlines several applications using this marine-type oxygen carrier for large biomanufacturing. It is a promising cell culture additive according to the increasing demand for therapeutic products such as monoclonal antibodies.
引用
收藏
页码:186 / 195
页数:10
相关论文
共 16 条
  • [1] Quantitative definition and monitoring of the host cell protein proteome using iTRAQ - a study of an industrial mAb producing CHO-S cell line
    Chiverton, Lesley M.
    Evans, Caroline
    Pandhal, Jagroop
    Landels, Andrew R.
    Rees, Byron J.
    Levison, Peter R.
    Wright, Phillip C.
    Smales, C. Mark
    BIOTECHNOLOGY JOURNAL, 2016, 11 (08) : 1014 - 1024
  • [2] Design, construction, and expression of recombinant human interferon beta gene in CHO-s cell line using EBV-based expression system
    Shayesteh, Mohadeseh
    Ghasemi, Fahimeh
    Tabandeh, Fatemeh
    Yakhchali, Bagher
    Shakibaie, Mehdi
    RESEARCH IN PHARMACEUTICAL SCIENCES, 2020, 15 (02) : 144 - 153
  • [3] Efficient Production of sTNFRII-gAD Fusion Protein in Large Quantity by Use of the Modified CHO-S Cell Expression System
    Cai, Qinzhen
    Zhao, Ai
    Yin, Yuting
    Ma, Lisha
    Jiao, Zhenzhen
    Zhi, Huilin
    Lai, Shouhua
    Cheng, Sha
    Yang, Hongmei
    Lu, Yinxiang
    Siminovitch, Katherine A.
    Gao, Jimin
    PLOS ONE, 2014, 9 (10):
  • [4] Optimized dual assay for the transgenes selection and screening in CHO cell line development for recombinant protein production
    Beketova, Elena V.
    Ibneeva, Liliia R.
    Abdulina, Yulia A.
    Dergousova, Elena A.
    Filatov, Vladimir L.
    Kozlovsky, Stanislav V.
    Shilov, Evgeny S.
    Datskevich, Petr N.
    Rozov, Fedor N.
    BIOTECHNOLOGY LETTERS, 2019, 41 (8-9) : 929 - 939
  • [5] Enhanced growth and recombinant protein production of Escherichia coli by a perfluorinated oxygen carrier in miniaturized fed-batch cultures
    Maciej Pilarek
    Julia Glazyrina
    Peter Neubauer
    Microbial Cell Factories, 10
  • [6] Investigating the metabolic load of monoclonal antibody production conveyed to an inducible CHO cell line using a transfer-rate online monitoring system
    Reyes, Sebastian-Juan
    Lemire, Lucas
    Durocher, Yves
    Voyer, Robert
    Henry, Olivier
    Pham, Phuong Lan
    JOURNAL OF BIOTECHNOLOGY, 2025, 399 : 47 - 62
  • [7] Establishment of a mammalian cell line suitable for industrial production of recombinant protein using mutations induced by high-energy beam radiation
    Chida, Yasuhito
    Takagi, Keiichi
    Terada, Satoshi
    CYTOTECHNOLOGY, 2013, 65 (06) : 955 - 965
  • [8] Production of a recombinant phospholipase A2 in Escherichia coli using resonant acoustic mixing that improves oxygen transfer in shake flasks
    Valdez-Cruz, Norma A.
    Reynoso-Cereceda, Greta I.
    Perez-Rodriguez, Saumel
    Restrepo-Pineda, Sara
    Gonzalez-Santana, Jesus
    Olvera, Alejandro
    Zavala, Guadalupe
    Alagon, Alejandro
    Trujillo-Roldan, Mauricio A.
    MICROBIAL CELL FACTORIES, 2017, 16
  • [9] Production of a recombinant phospholipase A2 in Escherichia coli using resonant acoustic mixing that improves oxygen transfer in shake flasks
    Norma A. Valdez-Cruz
    Greta I. Reynoso-Cereceda
    Saumel Pérez-Rodriguez
    Sara Restrepo-Pineda
    Jesus González-Santana
    Alejandro Olvera
    Guadalupe Zavala
    Alejandro Alagón
    Mauricio A. Trujillo-Roldán
    Microbial Cell Factories, 16
  • [10] Effect of hypoxia duration on the oxygen-dependent production of a recombinant protein, β-galactosidase, by an animal cell line, F6D2, with a hypoxia-inducible enhancer
    Yoshihito Shirai
    Mikio Inagaki
    Masaaki Yamaguchi
    Taiho Kambe
    Masaya Nagao
    Seiji Masuda
    Ryuzo Sasaki
    Cytotechnology, 1997, 25 : 71 - 77