Ghosh Srikanta, Joseph Simpson
4102 Urey Hall, Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0314, USA.
RNA. 2005 May;11(5):657-67. doi: 10.1261/rna.7224305. Epub 2005 Apr 5.
Ribosomes are composed of RNA and protein molecules that associate together to form a supramolecular machine responsible for protein biosynthesis. Detailed information about the structure of the ribosome has come from the recent X-ray crystal structures of the ribosome and the ribosomal subunits. However, the molecular interactions between the rRNAs and the r-proteins that occur during the intermediate steps of ribosome assembly are poorly understood. Here we describe a modification-interference approach to identify nonbridging phosphate oxygens within 16S rRNA that are important for the in vitro assembly of the Escherichia coli 30S small ribosomal subunit and for its association with the 50S large ribosomal subunit. The 30S small subunit was reconstituted from phosphorothioate-substituted 16S rRNA and small subunit proteins. Active 30S subunits were selected by their ability to bind to the 50S large subunit and form 70S ribosomes. Analysis of the selected population shows that phosphate oxygens at specific positions in the 16S rRNA are important for either subunit assembly or for binding to the 50S subunit. The X-ray crystallographic structures of the 30S subunit suggest that some of these phosphate oxygens participate in r-protein binding, coordination of metal ions, or for the formation of intersubunit bridges in the mature 30S subunit. Interestingly, however, several of the phosphate oxygens identified in this study do not participate in any interaction in the mature 30S subunit, suggesting that they play a role in the early steps of the 30S subunit assembly.
核糖体由RNA和蛋白质分子组成,它们结合在一起形成一个负责蛋白质生物合成的超分子机器。关于核糖体结构的详细信息来自最近核糖体及其亚基的X射线晶体结构。然而,在核糖体组装的中间步骤中,rRNA和r蛋白之间的分子相互作用却知之甚少。在此,我们描述了一种修饰干扰方法,以鉴定16S rRNA中对大肠杆菌30S小核糖体亚基的体外组装及其与50S大核糖体亚基的结合很重要的非桥连磷酸氧。30S小亚基由硫代磷酸取代的16S rRNA和小亚基蛋白重构而成。通过其与50S大亚基结合并形成70S核糖体的能力来选择有活性的30S亚基。对所选群体的分析表明,16S rRNA中特定位置的磷酸氧对亚基组装或与50S亚基的结合很重要。30S亚基的X射线晶体结构表明,其中一些磷酸氧参与r蛋白结合、金属离子配位或在成熟30S亚基中形成亚基间桥。然而,有趣的是,本研究中鉴定出的几个磷酸氧在成熟30S亚基中不参与任何相互作用,这表明它们在30S亚基组装的早期步骤中起作用。