背景(考古学)
生产力
合成生物学
生产(经济)
托换
代谢工程
生化工程
产品(数学)
产量(工程)
生物技术
生物
工程类
计算生物学
经济
生物化学
几何学
数学
材料科学
冶金
酶
古生物学
土木工程
宏观经济学
作者
Stefanie Dietmair,Lars K. Nielsen,Nicholas Timmins
摘要
Abstract Mammalian cells are the preferred host for the manufacture of a wide range of biopharmaceuticals, but production costs are high owing to low productivity. A range of rational engineering strategies have been pursued in order to increase volumetric product titres from mammalian cells, such as delaying apoptosis, manipulation of the cell cycle, and improving metabolism and protein processing. Unfortunately, outcomes from these strategies have been mixed, with few instances where significant improvements in product yield have been achieved. This article reviews and contrasts many of the engineering strategies attempted to date, highlighting the variability and context specificity in outcome. The paper argues that this is a reflection of the complexity of mammalian cells, and that a deeper understanding of the biology underpinning protein production for biotechnological purposes is required. Copyright © 2011 Society of Chemical Industry
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