首页> 外文期刊>Nucleic acids research >Ribosomal protein - nucleic acid interactions. I. Isolation of a polypeptide fragment from 30S protein S8 which binds to 16S rRNA
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Ribosomal protein - nucleic acid interactions. I. Isolation of a polypeptide fragment from 30S protein S8 which binds to 16S rRNA

机译:核糖体蛋白-核酸相互作用。 I.从与16S rRNA结合的30S蛋白S8中分离多肽片段

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Within the bacterial ribosome a large number of specific protein and rRNA interactions appear to be required for assembly of the particle and its subsequent function in protein synthesis. In this communication it is shown that it is possible to isolate cyanogen bromide digestion products from ribo-somal 30S protein S8 which will interact stoichiometrically with 16S rRNA. In addition to this a small binding polypeptide was generated from S8–16S rRNA complexes which were treated with proteinase K. The digestion of the complex yields a “protected” fragment of protein S8 which binds to 16S-rRNA. The isolated fragment will reassociate with 16S rRNA. It is not displaced by other 30S ribosomal proteins and blocks the binding of intact S8 to 16S rRNA. The size and possible structure of the S8 protein binding site are discussed and compared with the binding of cyanogen bromide digestion products which bind to 16S rRNA.
机译:在细菌核糖体内,颗粒的组装及其随后在蛋白质合成中的功能看来需要大量的特定蛋白质和rRNA相互作用。在这种交流中,表明可以从核糖体30S蛋白S8中分离出溴化氰消化产物,该产物将与16S rRNA发生化学计量相互作用。除此之外,还用蛋白酶K处理过的S8-16S rRNA复合物产生了一个小的结合多肽。复合物的消化产生了结合了16S-rRNA的S8蛋白的“受保护”片段。分离的片段将与16S rRNA重新关联。它不会被其他30S核糖体蛋白取代,并会阻止完整的S8与16S rRNA的结合。讨论了S8蛋白结合位点的大小和可能的结构,并将其与结合16S rRNA的溴化氰消化产物的结合进行了比较。

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