Strege M A, Lagu A L
Lilly Research Laboratories, A Division of Eli Lilly and Co., Indianapolis, Indiana 46285.
Anal Biochem. 1993 May 1;210(2):402-10. doi: 10.1006/abio.1993.1214.
Separations of model proteins obtained under denaturing conditions in the presence of micellar concentrations of ionic surfactants displayed high resolution and efficiency using either bare silica or C18-derivatized silica capillaries. Superior migration time reproducibility was achieved through the use of the C18-derivatized capillaries (run-to-run migration time % RSD = 0.2), relative to that obtained in bare silica capillaries (run-to-run migration time % RSD = 2.2), in the absence of buffer replenishment. The effects of surfactant concentration and pH upon the separation of a mixture of five model proteins of varying ionic and hydrophobic character were investigated, and the application of this technique to the analysis of a recombinant DNA-derived protein in fermentation broth was demonstrated.
在胶束浓度的离子表面活性剂存在下,于变性条件下对模型蛋白进行分离时,使用裸硅胶或C18衍生化硅胶毛细管均显示出高分辨率和高效率。相对于在不补充缓冲液的情况下在裸硅胶毛细管中获得的结果(每次运行的迁移时间%相对标准偏差=2.2),通过使用C18衍生化毛细管实现了更好的迁移时间重现性(每次运行的迁移时间%相对标准偏差=0.2)。研究了表面活性剂浓度和pH对五种具有不同离子和疏水特性的模型蛋白混合物分离的影响,并证明了该技术在发酵液中重组DNA衍生蛋白分析中的应用。