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Recombinant protein production by large-scale transient gene expression in mammalian cells: state of the art and future perspectives
Authors:Lucia Baldi  David L. Hacker  Myriam Adam  Florian M. Wurm
Affiliation:Laboratory of Cellular Biotechnology, Ecole Polytechnique Fédérale de Lausanne, Station 6, 1015, Lausanne, Switzerland. Lucia.Baldi@epfl.ch
Abstract:The expansion of the biologics pipeline depends on the identification of candidate proteins for clinical trials. Speed is one of the critical issues, and the rapid production of high quality, research-grade material for preclinical studies by transient gene expression (TGE) is addressing this factor in an impressive way: following DNA transfection, the production phase for TGE is usually 2-10 days. Recombinant proteins (r-proteins) produced by TGE can therefore enter the drug development and screening process in a very short time--weeks. With "classical" approaches to protein expression from mammalian cells, it takes months to establish a productive host cell line. This article summarizes efforts in industry and academia to use TGE to produce tens to hundreds of milligrams of r-proteins for either fundamental research or preclinical studies.
Keywords:Mammalian cells  Non-viral gene delivery  Recombinant protein  Transient gene expression
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