详细信息

Understanding the intracellular effects of yeast extract on the enhancement of Fc-fusion protein production in Chinese hamster ovary cell culture  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Understanding the intracellular effects of yeast extract on the enhancement of Fc-fusion protein production in Chinese hamster ovary cell culture

作者:Hu, Dongdong[1];Sun, Yating[1];Liu, Xuping[1];Liu, Jintao[1];Zhang, Xintao[1];Zhao, Liang[1];Wang, Haibin[2];Tan, Wen-Song[1];Fan, Li[1]

机构:[1]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China;[2]Zhejiang Hisun Pharmaceut Co Ltd, Hangzhou 311404, Zhejiang, Peoples R China

年份:2015

卷号:99

期号:20

起止页码:8429

外文期刊名:APPLIED MICROBIOLOGY AND BIOTECHNOLOGY

收录:;EI(收录号:20153901304350);WOS:【SCI-EXPANDED(收录号:WOS:000361493200010)】;

基金:This work was supported by the National Natural Science Foundation of China (Nos. 21206040 and 21406066), the National Science and Technology Major Project (No. 2013ZX10004003-003-003), and the National High Technology Research and Development Program of China (863 Program) (No. 2012AA02A303).

语种:英文

外文关键词:Chinese hamster ovary cells; Yeast extract; Fc-fusion protein; Specific productivity; Cell cycle arrest; mTOR

摘要:Yeast extract (YE), as a non-animal source additive for mammalian cell culture medium, has been widely used for manufacturing of therapeutic proteins. In the present study, one particular YE was found to have significantly improved the specific productivity (q (p)) of Fc-fusion protein in recombinant Chinese hamster ovary (rCHO) cell culture. In order to elucidate the intracellular effects of YE on protein productivity, steps of the target protein synthesis process were investigated to unveil their variations caused by YE addition. Stepwise analysis on Fc-fusion protein synthesis process showed that YE enhanced Fc-fusion protein gene transcription with cell cycle arrest at G1 phase; mammalian target of rapamycin (mTOR) signaling pathway was activated to enhance the translation of Fc-fusion protein, and the block in post-translational steps of Fc-fusion protein was alleviated by YE addition as well. Our results revealed the responses of multiple protein production steps to the addition of YE and provided a practical guidance for the separation and application of active compounds from hydrolysates.

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