Nygård O, Nika H
EMBO J. 1982;1(3):357-62. doi: 10.1002/j.1460-2075.1982.tb01174.x.
Protein constituents at the subunit interface of rat liver ribosomes were analysed by cross-linking with the bifunctional reagent, diepoxybutane (distance between reactive groups 4 A). Isolated 40S and 60S subunits were labelled with 125I and recombined with unlabelled complementary subunits. The two kinds of selectively labelled 80S ribosomes were treated with diepoxybutane at low concentration. Radioactive ribosomal proteins covalently attached to the rRNA of the unlabelled complementary subparticles were isolated by repeated gradient centrifugation. The RNA-bound, labelled proteins were identified by two-dimensional gel electrophoresis. The experiments showed that proteins S2, S3, S4, S6, S7, S13, and S14 in the small subunit of rat liver ribosomes are located at the ribosomal interface in close proximity to 28S rRNA. Similarly, proteins L3, L6, L7, and L8 were found at the the interface of the large ribosomal subunit in the close vicinity of 18S rRNA.
通过与双功能试剂1,4 - 丁二醇二缩水甘油醚(反应基团之间的距离为4 Å)交联,分析大鼠肝脏核糖体亚基界面处的蛋白质成分。分离出的40S和60S亚基用125I标记,并与未标记的互补亚基重组。两种选择性标记的80S核糖体用低浓度的1,4 - 丁二醇二缩水甘油醚处理。通过反复梯度离心分离与未标记互补亚基的rRNA共价连接的放射性核糖体蛋白。通过二维凝胶电泳鉴定与RNA结合的标记蛋白。实验表明,大鼠肝脏核糖体小亚基中的蛋白质S2、S3、S4、S6、S7、S13和S14位于核糖体界面,紧邻28S rRNA。同样,在大核糖体亚基的界面处,紧邻18S rRNA发现了蛋白质L3、L6、L7和L8。