生物生产
中国仓鼠卵巢细胞
生物
计算生物学
组学
卵巢
电流(流体)
生物信息学
生物技术
工程类
生物化学
遗传学
电气工程
受体
作者
Gino Stolfa,Matthew T. Smonskey,Ryan Boniface,Anna‐Barbara Hachmann,Paul Gulde,Atul Joshi,Anson Pierce,Scott J. Jacobia,Andrew M. Campbell
标识
DOI:10.1002/biot.201700227
摘要
CHO cells are the most prevalent platform for modern bio‐therapeutic production. Currently, there are several CHO cell lines used in bioproduction with distinct characteristics and unique genotypes and phenotypes. These differences limit advances in productivity and quality that can be achieved by the most common approaches to bioprocess optimization and cell line engineering. Incorporating omics‐based approaches into current bioproduction processes will complement traditional methodologies to maximize gains from CHO engineering and bioprocess improvements. In order to highlight the utility of omics technologies in CHO bioproduction, the authors discuss current applications as well as limitations of genomics, transcriptomics, proteomics, metabolomics, lipidomics, fluxomics, glycomics, and multi‐omics approaches and the potential they hold for the future of bioproduction. Multiple omics approaches are currently being used to improve CHO bioprocesses; however, the application of these technologies is still limited. As more CHO‐omic datasets become available and integrated into systems models, the authors expect significant gains in product yield and quality. While individual omics technologies provide incremental improvements in bioproduction, the authors will likely see the most significant gains by applying multi‐omics and systems biology approaches to individual CHO cell lines.
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