Politz S M, Glitz D G
Proc Natl Acad Sci U S A. 1977 Apr;74(4):1468-72. doi: 10.1073/pnas.74.4.1468.
Antibodies to the minor nucleoside N6,N6-dimethyladenosine have been used to map a unique location of the nucleoside in the small subunit of the Escherichia coli ribosome. Antibodies were induced in rabbits by a nucleoside-bovine albumin conjugate and shown to be highly specific for the dimethyladenosine hapten. The antibodies were shown to interact with 30S ribosomal subunits from strain PR7, but not with subunits from its mutant strain TPR201, which is resistant to kasugamycin and lacks the two successive residues of dimethyladenosine normally found near the 3'-end of E. coli 16S ribosomal RNA. Electron micrographs of strain PR7 subunits, crosslinked by single IgG molecules, show a single binding site on the surface of the ribosome. This binding site is consistent with observations relating the 3'-end of the ribosomal RNA, binding of initiation factor IF-3 and messenger RNA, and mapping of specific ribosomal proteins.
针对次要核苷N6,N6 - 二甲基腺苷的抗体已被用于确定该核苷在大肠杆菌核糖体小亚基中的独特位置。通过核苷 - 牛血清白蛋白偶联物在兔体内诱导产生抗体,并证明其对二甲基腺苷半抗原具有高度特异性。这些抗体显示与PR7菌株的30S核糖体亚基相互作用,但不与突变菌株TPR201的亚基相互作用,TPR201对春雷霉素具有抗性,并且缺少通常在大肠杆菌16S核糖体RNA 3'端附近发现的两个连续的二甲基腺苷残基。由单个IgG分子交联的PR7菌株亚基的电子显微镜照片显示核糖体表面有一个单一的结合位点。该结合位点与有关核糖体RNA的3'端、起始因子IF - 3和信使RNA的结合以及特定核糖体蛋白定位的观察结果一致。