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大肠杆菌素E3对核糖体RNA切割位点的定位。通过抗体-互补寡脱氧核苷酸复合物的电子显微镜观察确定其在小核糖体亚基上的位置。

Localization of the site of cleavage of ribosomal RNA by colicin E3. Placement on the small ribosomal subunit by electron microscopy of antibody--complementary oligodeoxynucleotide complexes.

作者信息

Lasater L S, Cann P A, Glitz D G

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Los Angeles 90024-1737.

出版信息

J Biol Chem. 1989 Dec 25;264(36):21798-805.

PMID:2689447
Abstract

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.

摘要

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。

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