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Characteristics of human cell line, F2N78, for the production of recombinant antibody in fed-batch and perfusion cultures.
Seo, Joon Serk; Min, Byung Sub; Kwon, Young-Bum; Lee, Soo-Young; Cho, Jong-Moon; Park, Keun-Hee; Yang, Yae Ji; Maeng, Ki Eun; Chang, Shin-Jae; Kim, Dong-Il.
Afiliación
  • Seo JS; Department of Biological Engineering, Inha University, Incheon 402-751, South Korea.
  • Min BS; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Kwon YB; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Lee SY; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Cho JM; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Park KH; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Yang YJ; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Maeng KE; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Chang SJ; R&D Center, Celltrion, Incheon 406-840, South Korea.
  • Kim DI; Department of Biological Engineering, Inha University, Incheon 402-751, South Korea. Electronic address: kimdi@inha.ac.kr.
J Biosci Bioeng ; 121(3): 317-24, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26454770
A human hybrid cell line, F2N78, was developed by somatic fusion of HEK293 and Namalwa cells for the production recombinant biopharmaceutical proteins. In this study, we performed perfusion culture to verify its potential in culture process used for human cell expression platform. Cell viability could be maintained over 90% and high viable cell density was obtained at higher than 1.0 × 10(7) cells/mL by bleeding process in perfusion culture. The cells were adapted well in both culture modes, but there were apparent differences in protein quality. Compared to fed-batch culture, degalactosylated forms such as G0F and G0 as well as Man5 showed no significant increases in perfusion culture. In terms of charge variants, acidic peaks increased, whereas main peaks constantly decreased according to the length of culture period in both methods.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Recombinantes / Técnicas de Cultivo de Célula / Técnicas de Cultivo Celular por Lotes / Células Híbridas / Anticuerpos Límite: Humans Idioma: En Revista: J Biosci Bioeng Asunto de la revista: ENGENHARIA BIOMEDICA / MICROBIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Corea del Sur Pais de publicación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Recombinantes / Técnicas de Cultivo de Célula / Técnicas de Cultivo Celular por Lotes / Células Híbridas / Anticuerpos Límite: Humans Idioma: En Revista: J Biosci Bioeng Asunto de la revista: ENGENHARIA BIOMEDICA / MICROBIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Corea del Sur Pais de publicación: Japón