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Large-scale transfection of mammalian cells.

Authors :
Baldi L
Hacker DL
Meerschman C
Wurm FM
Source :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2012; Vol. 801, pp. 13-26.
Publication Year :
2012

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.

Details

Language :
English
ISSN :
1940-6029
Volume :
801
Database :
MEDLINE
Journal :
Methods in molecular biology (Clifton, N.J.)
Publication Type :
Academic Journal
Accession number :
21987244
Full Text :
https://doi.org/10.1007/978-1-61779-352-3_2