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The main disadvantages of prokaryotic
expression systems, especially for
antibody expression, are the limited
glycosylation, folding, and secretion
capabilities of the host cells. Here, we
only focus on the characteristics of
antibody expression in E. coli which is the
almost exclusive prokaryotic production
system. Furthermore, Creative Biolabs
has established a novel prokaryotic
recombinant antibody production service
by our magic™ platform.
To improve folding efficiency, several strategies for increasing the solubility of recombinant
proteins expressed in E. coli have been optimized. Proteins such as isomerases and chaperones
have been overexpressed, the bacterial growth has been performed at low temperatures and in
the presence of osmolytes and alcohols known for stimulating heat-shock response, and even
specific strains have been developed. By contrast, the optimization of medium composition and
fermentation conditions is often neglected in academia with the exception of labs performing
more industrial-oriented R&D. Very high yields of antibody fragments produced in E. coli are
mainly provided by high-cell density fermentation in bioreactors: the expression of a hapten-
specific scFv produced in a bioreactor leads to yields up to 1.2 g/L compared to 16.5 mg/L yield
of the same antibody obtained by optimized shake flask production, which can be mostly
addressed to the over 100-fold higher cell density in the bioreactor.

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Neutralizing Antibody

  • 1. The main disadvantages of prokaryotic expression systems, especially for antibody expression, are the limited glycosylation, folding, and secretion capabilities of the host cells. Here, we only focus on the characteristics of antibody expression in E. coli which is the almost exclusive prokaryotic production system. Furthermore, Creative Biolabs has established a novel prokaryotic recombinant antibody production service by our magic™ platform. To improve folding efficiency, several strategies for increasing the solubility of recombinant proteins expressed in E. coli have been optimized. Proteins such as isomerases and chaperones have been overexpressed, the bacterial growth has been performed at low temperatures and in the presence of osmolytes and alcohols known for stimulating heat-shock response, and even specific strains have been developed. By contrast, the optimization of medium composition and fermentation conditions is often neglected in academia with the exception of labs performing more industrial-oriented R&D. Very high yields of antibody fragments produced in E. coli are mainly provided by high-cell density fermentation in bioreactors: the expression of a hapten- specific scFv produced in a bioreactor leads to yields up to 1.2 g/L compared to 16.5 mg/L yield of the same antibody obtained by optimized shake flask production, which can be mostly addressed to the over 100-fold higher cell density in the bioreactor.