|Journal of Molecular Microbiology and Biotechnology (2002) 4(6):519-24|
|Northeast Structural Genomics Consortium|
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Protein misfolding resulting in the formation of inclusion bodies is one of the major problems during protein overexpression in Escherichia coil. ...
In this paper, we introduce a new method, which is simply to heat shock a cell culture prior to protein induction, allowing effective enhancement of the solubility and thereby the yield of overexpressed proteins in E. coli. Using this method, we show that the solubility of the E. coli protein KsgA-AN is significantly increased when overexpressed from a T7 promoter. In addition, we also show that the solubility of several Caenorhabditis elegans proteins are also enhanced after heat-shock treatment when expressed in E. coli. Taken together, these results suggest that the "heat-shock protocol" is a generalizable and useful method for increasing the solubility of many proteins overexpressed in E. coli.
|methods genetics metabolism chemistry physiology |
|Heat-Shock Response Escherichia coli Solubility Culture Media Caenorhabditis elegans Proteins Animals Biotechnology Methyltransferases |
|27 (Last update: 03/18/2017 11:47:11am)|
|J Mol Microbiol Biotechnol. 2002 Nov;4(6):519-24.|