Yadav Deepak Kumar, Lukavsky Peter J
Central European Institute of Technology, Masaryk University, Kamenice 753/5, 62500 Brno, Czech Republic.
Central European Institute of Technology, Masaryk University, Kamenice 753/5, 62500 Brno, Czech Republic.
Prog Nucl Magn Reson Spectrosc. 2016 Nov;97:57-81. doi: 10.1016/j.pnmrs.2016.10.001. Epub 2016 Oct 27.
Structure determination of RNA-protein complexes is essential for our understanding of the multiple layers of RNA-mediated posttranscriptional regulation of gene expression. Over the past 20years, NMR spectroscopy became a key tool for structural studies of RNA-protein interactions. Here, we review the progress being made in NMR structure determination of large ribonucleoprotein assemblies. We discuss approaches for the design of RNA-protein complexes for NMR structural studies, established and emerging isotope and segmental labeling schemes suitable for large RNPs and how to gain distance restraints from NOEs, PREs and EPR and orientational information from RDCs and SAXS/SANS in such systems. The new combination of NMR measurements with MD simulations and its potential will also be discussed. Application and combination of these various methods for structure determination of large RNPs will be illustrated with three large RNA-protein complexes (>40kDa) and other interesting complexes determined in the past six and a half years.
RNA-蛋白质复合物的结构测定对于我们理解RNA介导的基因表达转录后调控的多个层面至关重要。在过去20年中,核磁共振光谱法成为RNA-蛋白质相互作用结构研究的关键工具。在此,我们综述了大型核糖核蛋白组装体核磁共振结构测定方面取得的进展。我们讨论了用于核磁共振结构研究的RNA-蛋白质复合物设计方法、适用于大型核糖核蛋白的已确立和新兴的同位素及片段标记方案,以及如何在此类系统中从核Overhauser效应(NOEs)、顺磁弛豫增强(PREs)和电子顺磁共振(EPR)获得距离限制,从残余偶极耦合(RDCs)和小角X射线散射/小角中子散射(SAXS/SANS)获得取向信息。还将讨论核磁共振测量与分子动力学(MD)模拟的新组合及其潜力。将通过过去六年半内测定的三个大型RNA-蛋白质复合物(>40 kDa)及其他有趣的复合物来说明这些用于大型核糖核蛋白结构测定的各种方法的应用和组合。