Noguère Christophe, Larsson Anna M, Guyot Jean-Christophe, Bignon Christophe
Architecture et Fonction des Macromolécules Biologiques (AFMB), UMR 7257 CNRS and Aix-Marseille University, Marseille, France.
Protein Expr Purif. 2012 Aug;84(2):204-13. doi: 10.1016/j.pep.2012.05.011. Epub 2012 Jun 15.
Producing recombinant proteins in Escherichia coli (E. coli) is generally performed using a trial and error approach with the different expression variables being tested independently from each other. As a consequence, variable interactions are lost which makes the trial and error approach quite time-consuming. In this paper, we report how switching from a trial and error to a fractional factorial approach allows testing in less than 2 weeks four expression variables (E. coli strains, culture media, expression temperatures and N-terminal fusion tags) in a single experiment. The method, called "Fusion-InFFact", was validated using four test proteins. In all cases, Fusion-InFFact allowed finding conditions for expressing high yields of soluble proteins. The method was originally set-up for high throughput structural genomics programs, but can be used in any recombinant protein expression project.
在大肠杆菌(E. coli)中生产重组蛋白通常采用反复试验的方法,对不同的表达变量进行独立测试。因此,变量之间的相互作用被忽略了,这使得反复试验的方法非常耗时。在本文中,我们报告了从反复试验方法转换为分数析因法如何能够在不到两周的时间内,在单个实验中对四个表达变量(大肠杆菌菌株、培养基、表达温度和N端融合标签)进行测试。这种方法称为“Fusion-InFFact”,已通过四种测试蛋白进行了验证。在所有情况下,Fusion-InFFact都能找到表达高产率可溶性蛋白的条件。该方法最初是为高通量结构基因组学项目建立的,但可用于任何重组蛋白表达项目。