Lasater L S, Cann P A, Glitz D G
Department of Biological Chemistry, School of Medicine, University of California, Los Angeles 90024-1737.
J Biol Chem. 1989 Dec 25;264(36):21798-805.
Colicin E3 is a ribonuclease that inactivates Escherichia coli ribosomes by cleaving the RNA of the small ribosomal subunit after nucleotide 1493. A series of oligodeoxynucleotides that complement 16 S RNA in the region of the colicin cleavage site has been synthesized, and their ability to form complexes with 30 S ribosomal subunits has been measured using a nitrocellulose filter-binding assay. The most efficiently bound probe, complementary to residues 1485-1496, was modified with antibody-recognizable derivatives at the 5'-end, the 3'-end, or both. Antibody-oligonucleotide-subunit complexes were then generated and examined by electron microscopy. Antibody binding was seen at the tip of the platform of the 30 S subunit. The complementary oligonucleotide and thus the site at which colcin E3 cleavage occurs is therefore in the same physical region as the 3'-end of the 16 S ribosomal RNA and its message-positioning "Shine-Dal-garno" sequence.
大肠杆菌素E3是一种核糖核酸酶,它通过切割小核糖体亚基中核苷酸1493之后的RNA来使大肠杆菌核糖体失活。已经合成了一系列在大肠杆菌素切割位点区域与16S RNA互补的寡脱氧核苷酸,并使用硝酸纤维素滤膜结合试验测定了它们与30S核糖体亚基形成复合物的能力。与残基1485 - 1496互补的结合效率最高的探针在5'端、3'端或两端用可被抗体识别的衍生物进行了修饰。然后生成抗体 - 寡核苷酸 - 亚基复合物并通过电子显微镜检查。在30S亚基平台的顶端可见抗体结合。因此,互补寡核苷酸以及大肠杆菌素E3切割发生的位点与16S核糖体RNA的3'端及其信息定位“Shine - Dalgarno”序列处于相同的物理区域。