O'Callaghan Peter M, James David C
Department of Chemical and Process Engineering, University of Sheffield, Mappin St., Sheffield S1 3JD, UK.
Brief Funct Genomic Proteomic. 2008 Mar;7(2):95-110. doi: 10.1093/bfgp/eln012. Epub 2008 Mar 7.
The increasing demand for recombinant therapeutic proteins has placed significant pressure on the biopharmaceutical industry to develop high-yielding, mammalian cell-based production systems. Current efforts to increase the production of recombinant proteins by mammalian host cells largely proceed by the lengthy screening of clonal derivatives rather than by directed genetic or metabolic engineering. However, the advent of systems biology has created a new set of tools that will ensure that future engineering strategies will be informed by an understanding of the genetic/regulatory and metabolic networks that determine the functional competence of mammalian cell factories in vitro. In this review we summarize recent systems-level studies that utilize genome-scale analytical tools to analyse the functional basis for key production process characteristics such as high cell-specific productivity, correct product processing and rapid cell proliferation in the in vitro environment. We also describe the use of high-throughput -omic technologies to investigate how mammalian cell factories respond to environmental and metabolic perturbation.
对重组治疗性蛋白日益增长的需求给生物制药行业带来了巨大压力,促使其开发高产的基于哺乳动物细胞的生产系统。目前,通过哺乳动物宿主细胞提高重组蛋白产量的努力主要是通过对克隆衍生物进行冗长的筛选,而不是通过定向基因工程或代谢工程。然而,系统生物学的出现创造了一套新工具,这将确保未来的工程策略能够基于对遗传/调控和代谢网络的理解,这些网络决定了体外哺乳动物细胞工厂的功能能力。在这篇综述中,我们总结了最近的系统水平研究,这些研究利用基因组规模的分析工具来分析关键生产过程特征的功能基础,如高细胞特异性生产力、正确的产物加工以及体外环境中的快速细胞增殖。我们还描述了如何使用高通量组学技术来研究哺乳动物细胞工厂对环境和代谢扰动的反应。