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首页> 外文期刊>Nucleic acids research >New RNA-protein crosslinks in domains 1 and 2 of E.coli 30S ribosomal subunits obtained by means of an intrinsic photoaffinity probe
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New RNA-protein crosslinks in domains 1 and 2 of E.coli 30S ribosomal subunits obtained by means of an intrinsic photoaffinity probe

机译:通过内在光亲和探针获得的大肠杆菌30S核糖体亚基的结构域1和2中的新RNA-蛋白质交联

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Functionally active 705 ribosomes containing 4-thiouridine (s4U) in place of uridine were prepared by a formerly described in vivo substitution method. Proteins were crosslinked to RNA by 366nm photoactivation of s4U We observe the systematic and caracteristic formation of 30S dimers ; they were eliminated for analysis of RNA-protein crosslinks. M13 probes containing rDNA inserts complementary to domains 1 and 2 of 16S RNA from the 5end up to nucleotide 868 were used to select contiquous or overlapping RNA sections. The proteins covalently crosslinked to each RNA section were identified as S3, S4, S5, S7, S9, S18, S20 and S21. Several crosslinks are compatible with previously published sites for proteins S5, S18, S20 and S21 ; others for proteins S3, S4, S7, S9, S18 correspond necessarily to new sites.
机译:通过先前描述的体内替代方法,制备了含有4-硫尿苷(s 4 U)代替尿苷的功能活性的705个核糖体。 s 4 U的366nm光活化将蛋白质与RNA交联。我们观察到30S二聚体的系统化和特征化形成;消除了它们,用于分析RNA-蛋白质交联。使用含有与5S直至核苷酸868的16S RNA的结构域1和2互补的rDNA插入片段的M13探针来选择连续或重叠的RNA片段。与每个RNA部分共价交联的蛋白质被鉴定为S3,S4,S5,S7,S9,S18,S20和S21。几个交联点与先前发布的蛋白质S5,S18,S20和S21的位点兼容;蛋白质S3,S4,S7,S9,S18的其他部分必须对应于新位点。

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