Manabe T
Department of Chemistry, Faculty of Science, Ehime University, Matsuyama, Japan.
Electrophoresis. 2000 Apr;21(6):1116-22. doi: 10.1002/(SICI)1522-2683(20000401)21:6<1116::AID-ELPS1116>3.0.CO;2-Z.
Analysis of proteins in complex mixtures such as cell lysates is presently performed by two-dimensional polyacrylamide gel electrophoresis under denaturing conditions (denaturing 2-D PAGE) followed by extraction of proteins from gel pieces and structural analysis of the proteins. This type of protein analysis is contributing to the correlation of information stored in DNA sequences with the structure of the product polypeptides. However, denaturing 2-D PAGE has its own limitations and it is necessary to develop various methods of protein analysis to reconstruct the total structure and function of proteins in complex systems. This review article summarizes the work in our laboratory to explore proteins in human plasma combining various electrophoretic techniques: nondenaturing and denaturing 2-D PAGE, capillary electrophoresis, and agarose gel isoelectric focusing.
目前,对于细胞裂解液等复杂混合物中的蛋白质分析,是在变性条件下通过二维聚丙烯酰胺凝胶电泳(变性二维聚丙烯酰胺凝胶电泳)进行的,随后从凝胶块中提取蛋白质并对其进行结构分析。这种蛋白质分析方法有助于将DNA序列中存储的信息与产物多肽的结构相关联。然而,变性二维聚丙烯酰胺凝胶电泳有其自身的局限性,因此有必要开发各种蛋白质分析方法,以重建复杂系统中蛋白质的整体结构和功能。这篇综述文章总结了我们实验室结合各种电泳技术(非变性和变性二维聚丙烯酰胺凝胶电泳、毛细管电泳和琼脂糖凝胶等电聚焦)探索人血浆中蛋白质的工作。