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哺乳动物细胞的大规模转染

Large-scale transfection of mammalian cells.

作者信息

Baldi Lucia, Hacker David L, Meerschman Carine, Wurm Florian M

机构信息

Laboratory of Cellular Biotechnology, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

出版信息

Methods Mol Biol. 2012;801:13-26. doi: 10.1007/978-1-61779-352-3_2.

Abstract

The large-scale transfection of mammalian cells allows moderate (milligram to gram) amounts of recombinant proteins (r-proteins) to be obtained for fundamental or clinical research. In this article, we describe a one-liter transfection using polyethyleneimine (PEI) for DNA delivery into human embryonic kidney (HEK-293) cells cultivated in serum-free suspension to produce a recombinant human monoclonal antibody that yields up to about 1 g/L in a 10-day process. The method is based on a DNA delivery step performed at high cell density (20×10(6) cells/mL) by direct addition of DNA and PEI to the culture. Subsequently, the cells are diluted 20-fold for the 10-day production phase in the presence of valproic acid (VPA), a histone deacetylase inhibitor. The methods for plasmid purification, antibody quantification by enzyme-linked immunosorbent assay (ELISA), and affinity purification with protein A are also described.

摘要

对哺乳动物细胞进行大规模转染,能够获取适量(毫克至克级)的重组蛋白用于基础研究或临床研究。在本文中,我们描述了一种使用聚乙烯亚胺(PEI)将DNA导入无血清悬浮培养的人胚肾(HEK-293)细胞中的一升规模转染方法,以生产一种重组人单克隆抗体,在为期10天的过程中产量可达约1 g/L。该方法基于在高细胞密度(20×10⁶个细胞/mL)下通过直接向培养物中添加DNA和PEI来进行DNA递送步骤。随后,在组蛋白去乙酰化酶抑制剂丙戊酸(VPA)存在的情况下,将细胞稀释20倍进行为期10天的生产阶段。文中还介绍了质粒纯化方法、通过酶联免疫吸附测定(ELISA)进行抗体定量以及使用蛋白A进行亲和纯化的方法。

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