Raj N B, Ro-Choi T S, Busch H
Biochemistry. 1975 Oct 7;14(20):4380-5. doi: 10.1021/bi00691a006.
Nuclear ribonucleoprotein (RNP) complexes that contain the U1 and U2 RNA of chromatin of Novikoff hepatoma cells were extracted with 0.01 M Tris-HCl (pH 8.0) after the nuclei were initially washed with 0.075 M NaCl and 0.025 M EDTA (pH 8.0). These RNP complexes were purified by chromatography on Sepharose 6B columns and centrifugation on sucrose density gradients. The identity of the U1 and U2 RNA in these particles was established by their electrophoretic mobility in polyacrylamide gels and their T1 RNase fingerprints which were identical with those of authentic U1 and U2 RNA (R. Reddy et al. (1974), J. Biol. Chem.249, 6486-6494; H. Shibata et al. (1974), Mol. Cell. Biochem. 4, 3-19). The nuclear riboncleoproteins had a buoyant density of 1.47 g/ml in CsCl gradients. Two-dimensional polyacrylamide gel electrophoresis of their proteins showed these RNP complexes contain 10 polypeptide spots, of which two are phosphorylated in vivo.
在用0.075 M NaCl和0.025 M EDTA(pH 8.0)初步洗涤细胞核后,用0.01 M Tris-HCl(pH 8.0)提取诺维科夫肝癌细胞核中含有U1和U2 RNA的核糖核蛋白(RNP)复合物。这些RNP复合物通过在琼脂糖6B柱上进行层析和在蔗糖密度梯度上进行离心来纯化。这些颗粒中U1和U2 RNA的身份通过它们在聚丙烯酰胺凝胶中的电泳迁移率以及它们的T1核糖核酸酶指纹图谱得以确定,这些指纹图谱与 authentic U1和U2 RNA的指纹图谱相同(R. Reddy等人(1974年),《生物化学杂志》249, 6486 - 6494;H. Shibata等人(1974年),《分子细胞生物化学》4, 3 - 19)。在CsCl梯度中,核糖核蛋白的浮力密度为1.47 g/ml。对其蛋白质进行的二维聚丙烯酰胺凝胶电泳显示,这些RNP复合物含有10个多肽斑点,其中两个在体内被磷酸化。