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利用 Semliki Forest 病毒表达系统大规模瞬时产生 5-HT3 受体。

Large scale transient 5-HT3 receptor production with the Semliki Forest Virus Expression System.

机构信息

Serono Pharmaceutical Research Institute, 14 Chemin des Aulx, CH-1228, Plan-les-Ouates, Switzerland,

出版信息

Cytotechnology. 2000 Mar;32(3):199-208. doi: 10.1023/A:1008192709549.

Abstract

The expression of recombinant proteins with the Semliki Forest Virus (SFV) system has been scaled up to bioreactor scale. As a model protein for this study the human 5-HT(3) receptor was chosen. The gene for the receptor was subcloned into the SFV expression plasmid pSFV1. Virus production by in vivo packaging and production of the recombinant protein was scaled up, the latter to a reactor volume of 11.5 l. A Vibromix(TM) agitation system was chosen to overcome aggregation problems of BHK cells in suspension. In the process, cells were first grown to a density of 10(6) cells/ml, the medium was then exchanged with fresh medium and the culture was infected with the recombinant virus at an estimated multiplicity of infection of 30. 24 h post infection we measured an expression level of 3 million functional 5-HT(3) receptors per cell. For harvesting, the cells were pelleted by centrifugation. The receptor protein was purified in a single step (Hovius et al., 1998) by exploiting the hexa-His tag at minimal protein loss (51% yield). Experiments to optimise expression resulted in yields up to 8 million receptors per cell, when the pH of a suspension culture was controlled at pH 7.3. Rapid virus generation and protein production, high protein yields as well as successful large scale application have made the SFV expression system attractive to produce large quantities of recombinant protein in a very short time. After optimisation of the expression conditions (in particular by setting the pH at 7.3), yields were increased twofold.

摘要

利用 Semliki Forest 病毒 (SFV) 系统表达重组蛋白已经扩大到生物反应器规模。作为这项研究的模型蛋白,选择了人类 5-HT(3)受体。该受体的基因被亚克隆到 SFV 表达质粒 pSFV1 中。通过体内包装生产病毒和生产重组蛋白的规模都扩大了,后者扩大到 11.5 升的反应器体积。选择 Vibromix(TM)搅拌系统来克服悬浮 BHK 细胞的聚集问题。在这个过程中,细胞首先生长到 10(6)个细胞/ml 的密度,然后用新鲜培养基交换培养基,并以估计的感染复数 30 感染重组病毒。感染后 24 小时,我们测量到每个细胞有 300 万个功能性 5-HT(3)受体。为了收获,细胞通过离心沉淀。通过利用六组氨酸标签最小化蛋白损失(51%收率),在单个步骤中对受体蛋白进行纯化(Hovius 等人,1998)。优化表达的实验导致当悬浮培养物的 pH 控制在 pH 7.3 时,每个细胞的产量高达 800 万个受体。SFV 表达系统具有快速生成病毒和生产蛋白、高蛋白产量以及成功的大规模应用等优点,使其成为在短时间内大量生产重组蛋白的有吸引力的选择。优化表达条件(特别是将 pH 设置为 7.3)后,产量增加了两倍。

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