McWilliams R A, Glitz D G
Department of Biological Chemistry Institute, UCLA School of Medicine 90024-1737.
Biochimie. 1991 Jul-Aug;73(7-8):911-8. doi: 10.1016/0300-9084(91)90132-k.
Oligonucleotides that complement Escherichia coli 16S ribosomal RNA residues 685-696 and 694-705 have been synthesized so as to incorporate antibody-recognizable markers: a 3'-terminal residue of N6-delta 2-isopentenyladenosine, a 5'-dinitrophenyl group, or both. Each oligonucleotide is able to bind RNA within the small ribosomal subunit, whether free or in 70S ribosomes. Immune electron microscopy places probes at nucleotides 685, 694 and 705 within a single area, at the tip of the subunit platform, very near the position of the 3'-end of the 16S RNA.
已合成与大肠杆菌16S核糖体RNA 685 - 696位和694 - 705位残基互补的寡核苷酸,以便掺入可被抗体识别的标记:N6 - δ2 - 异戊烯基腺苷的3'末端残基、5' - 二硝基苯基或两者。每个寡核苷酸都能够结合小核糖体亚基内的RNA,无论其是游离的还是存在于70S核糖体中。免疫电子显微镜将探针定位在单个区域内的685、694和705位核苷酸处,位于亚基平台的尖端,非常靠近16S RNA 3'末端的位置。