Issinger O G, Beier H
Mol Gen Genet. 1978 Apr 17;160(3):297-309. doi: 10.1007/BF00332973.
Electrophoresis of ribosomal proteins according to Kaltschmidt and Wittmann, 1970a, b (pH 8.6/pH 4.5 urea system) yielded 29 proteins for the small subunits and 35 and 37 proteins for the large subunits of Krebs II ascites and HeLa ribosomes, respectively. Analysis of the proteins according to a modified technique by Mets and Bogorad (1974) (pH 4.5/pH 8.6 SDS system) revealed 28 and 29 proteins in the small subunits and 37 and 38 proteins in the large subunits of Krebs II ascites and HeLa ribosomes. The molecular weights of the individual proteins were determined by: 1. "three-dimensional" gel electrophoresis; 2. two-dimensional gel electrophoresis at pH 4.K/pH 8.6 in SDS. The molecular weights for 40S proteins ranged from 10,000 to 39,000 dalton (number average molecular weight: 21,000). The molecular weights for the 60S proteins ranged from 14,000 to 44,000 dalton (number average molecular weight: 23,000) using the "three-dimensional" technique. A molecular weight range from 10,000 to 38,000 dalton (number average molecular weight: 21,000) was obtained for the 40S subunits, whereas the molecular weights for the 60S ribosomal proteins (average molecular weight: 26,000) ranged from 12,000 to 69,000 dalton using the pH 4.5/pH 8.6 SDS system. The molecular weights Krebs II ascites and HeLa ribosomal proteins are compared with those obtained by other authors for different mammalian species.
根据卡尔施密特和维特曼(1970a,b)的方法(pH 8.6/pH 4.5尿素系统)对核糖体蛋白进行电泳分析,结果显示,克雷布斯II腹水瘤核糖体和海拉细胞核糖体的小亚基分别有29种蛋白,大亚基分别有35种和37种蛋白。按照梅茨和博戈拉德(1974)改进的技术(pH 4.5/pH 8.6 SDS系统)对这些蛋白进行分析,结果显示,克雷布斯II腹水瘤核糖体和海拉细胞核糖体的小亚基分别有28种和29种蛋白,大亚基分别有37种和38种蛋白。通过以下方法测定了各个蛋白的分子量:1. “三维”凝胶电泳;2. 在pH 4.5/pH 8.6的SDS中进行二维凝胶电泳。40S蛋白的分子量范围为10,000至39,000道尔顿(数均分子量:21,000)。使用“三维”技术时,60S蛋白的分子量范围为14,000至44,000道尔顿(数均分子量:23,000)。对于40S亚基,分子量范围为10,000至38,000道尔顿(数均分子量:21,000),而使用pH 4.5/pH 8.6 SDS系统时,60S核糖体蛋白的分子量(平均分子量:26,000)范围为12,000至69,000道尔顿。将克雷布斯II腹水瘤核糖体和海拉细胞核糖体蛋白的分子量与其他作者针对不同哺乳动物物种所获得的分子量进行了比较。