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Cryo-electron microscopy snapshots of the spliceosome: structural insights into a dynamic ribonucleoprotein machine
Nature Structural & Molecular Biology ( IF 12.5 ) Pub Date : , DOI: 10.1038/nsmb.3463 Sebastian M Fica , Kiyoshi Nagai
Nature Structural & Molecular Biology ( IF 12.5 ) Pub Date : , DOI: 10.1038/nsmb.3463 Sebastian M Fica , Kiyoshi Nagai
The spliceosome excises introns from pre-messenger RNAs using an RNA-based active site that is cradled by a dynamic protein scaffold. A recent revolution in cryo-electron microscopy (cryo-EM) has led to near-atomic-resolution structures of key spliceosome complexes that provide insight into the mechanism of activation, splice site positioning, catalysis, protein rearrangements and ATPase-mediated dynamics of the active site. The cryo-EM structures rationalize decades of observations from genetic and biochemical studies and provide a molecular framework for future functional studies.
中文翻译:
剪接体的低温电子显微镜快照:动态核糖核蛋白机器的结构见解
剪接体使用由动态蛋白支架支撑的基于RNA的活性位点从信使前RNA中切除内含子。低温电子显微镜(cryo-EM)的最新革命已导致关键剪接体复合物的接近原子分辨率的结构,从而提供了对激活机制,剪接位点定位,催化,蛋白质重排和ATPase介导的PPAR动力学的深入了解。活动站点。cryo-EM结构合理化了数十年来遗传和生化研究的观察结果,并为未来的功能研究提供了分子框架。
更新日期:2017-10-11
中文翻译:
剪接体的低温电子显微镜快照:动态核糖核蛋白机器的结构见解
剪接体使用由动态蛋白支架支撑的基于RNA的活性位点从信使前RNA中切除内含子。低温电子显微镜(cryo-EM)的最新革命已导致关键剪接体复合物的接近原子分辨率的结构,从而提供了对激活机制,剪接位点定位,催化,蛋白质重排和ATPase介导的PPAR动力学的深入了解。活动站点。cryo-EM结构合理化了数十年来遗传和生化研究的观察结果,并为未来的功能研究提供了分子框架。