Suppr超能文献

一种在 CHO 细胞中进行瞬时基因表达的简单、高产的方法。

A simple high-yielding process for transient gene expression in CHO cells.

机构信息

Laboratory for Cellular Biotechnology (LBTC), École Polytechnique Fédéral de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.

出版信息

J Biotechnol. 2011 Apr 20;153(1-2):22-6. doi: 10.1016/j.jbiotec.2011.03.001. Epub 2011 Mar 15.

Abstract

Here we describe a simplified method for transient gene expression (TGE) in suspension-adapted Chinese hamster ovary (CHO) cells using polyethylenimine (PEI) for DNA delivery. Both the transfection and production phases of the bioprocess were performed at a density of 4 × 10⁶ cells/mL at 31 °C. In addition, the amounts of both PEI and plasmid DNA were reduced up to 50% on a per cell basis compared to previously published protocols from this laboratory, resulting in higher cell viability after transfection and higher volumetric recombinant protein yields. In batch cultures of up to 14 days, reproducible recombinant antibody yields up to 300 mg/L were achieved at small scale (5 mL) and up to 250 mg/L at large scale (500 mL). The simplicity and improved yields are expected to increase the utility of CHO cells for the rapid production of recombinant proteins at larger scales by TGE.

摘要

在这里,我们描述了一种使用聚乙烯亚胺(PEI)进行 DNA 递送的悬浮适应中国仓鼠卵巢(CHO)细胞瞬时基因表达(TGE)的简化方法。生物工艺的转染和生产阶段均在 31°C 下以 4×10⁶个细胞/mL 的密度进行。此外,与本实验室之前发表的方案相比,PEI 和质粒 DNA 的用量均减少了 50%,从而在转染后提高了细胞活力,并提高了体积重组蛋白的产量。在长达 14 天的分批培养中,在小规模(5 mL)时可实现高达 300 mg/L 的重现性重组抗体产量,在大规模(500 mL)时可实现高达 250 mg/L 的产量。这种方法的简单性和提高的产量有望增加 CHO 细胞在更大规模上通过 TGE 快速生产重组蛋白的实用性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验