Blanchard S C, Fourmy D, Eason R G, Puglisi J D
Department of Structural Biology, Stanford University School of Medicine Fairchild Center, California 94305-5400, USA.
Biochemistry. 1998 May 26;37(21):7716-24. doi: 10.1021/bi973125y.
Through an affinity chromatography based modification-interference assay, we have identified chemical groups within Escherichia coli 16S ribosomal RNA sequence that are required for binding the aminoglycoside antibiotic paromomycin. Paromomycin was covalently linked to solid support via a nine atom spacer from the 6"'-amine of ring IV, and chemical modifications to an A-site oligonucleotide that disrupted binding were identified. Positions in the RNA oligonucleotide that correspond to G1405(N7), G1491(N7), G1494(N7), A1408(N7), A1493(N7), A1408(N1), A1492(N1), and A1493(N1), as well as the pro-R phosphate oxygens of A1492 and A1493 in 16S rRNA are chemical groups that are essential for a high-affinity RNA-paromomycin interaction. These data are consistent with genetic, biochemical, and structural studies related to neomycin-class antibiotics and provide additional information for establishing an exact model for their interaction with the ribosome.
通过基于亲和色谱的修饰干扰试验,我们已鉴定出大肠杆菌16S核糖体RNA序列中与氨基糖苷类抗生素巴龙霉素结合所需的化学基团。巴龙霉素通过来自环IV的6''-胺的九个原子间隔臂与固相载体共价连接,并鉴定出对破坏结合的A位点寡核苷酸的化学修饰。RNA寡核苷酸中与16S rRNA中的G1405(N7)、G1491(N7)、G1494(N7)、A1408(N七)、A1493(N7)、A1408(N1)、A1492(N1)和A1493(N1)相对应的位置,以及A1492和A1493的前-R磷酸氧是高亲和力RNA-巴龙霉素相互作用所必需的化学基团。这些数据与新霉素类抗生素相关的遗传、生化和结构研究一致,并为建立它们与核糖体相互作用的确切模型提供了额外信息。