Fogel S, Sypherd P S
J Bacteriol. 1968 Aug;96(2):358-64. doi: 10.1128/jb.96.2.358-364.1968.
We have described a new method for the quantitative separation of ribosomal proteins and ribosomal ribonucleic acid. A procedure for the preparation of individual ribosomal proteins by polyacrylamide gel electrophoresis is also described. By the use of gels with smaller pores, at least four of the electrophoretic components from the 30S ribosome can be split into additional protein fractions. By the methods described here, it is possible to isolate in high purity at least 15 different proteins from the 30S ribosome of Escherichia coli.
我们描述了一种定量分离核糖体蛋白和核糖体核糖核酸的新方法。还描述了一种通过聚丙烯酰胺凝胶电泳制备单个核糖体蛋白的程序。通过使用孔径较小的凝胶,30S核糖体的至少四种电泳成分可进一步分离成其他蛋白组分。通过本文所述方法,有可能从大肠杆菌的30S核糖体中以高纯度分离出至少15种不同的蛋白质。