Center for Integrated Protein Science Munich, Department Chemie, Technical University of Munich, Lichtenbergstr. 4, 85748, Garching, Germany.
Institute of Structural Biology, Helmholtz Zentrum München, Ingolstadter Landstr. 1, 85764, Neuherberg, Germany.
Sci Rep. 2017 Jul 14;7(1):5393. doi: 10.1038/s41598-017-05821-z.
NMR spectroscopy is a powerful technique to study ribonucleic acids (RNAs) which are key players in a plethora of cellular processes. Although the NMR toolbox for structural studies of RNAs expanded during the last decades, they often remain challenging. Here, we show that solvent paramagnetic relaxation enhancements (sPRE) induced by the soluble, paramagnetic compound Gd(DTPA-BMA) provide a quantitative measure for RNA solvent accessibility and encode distance-to-surface information that correlates well with RNA structure and improves accuracy and convergence of RNA structure determination. Moreover, we show that sPRE data can be easily obtained for RNAs with any isotope labeling scheme and is advantageous regarding sample preparation, stability and recovery. sPRE data show a large dynamic range and reflect the global fold of the RNA suggesting that they are well suited to identify interaction surfaces, to score structural models and as restraints in RNA structure determination.
NMR 光谱学是一种强大的技术,可用于研究核糖核酸(RNAs),它们是众多细胞过程中的关键参与者。尽管用于 RNA 结构研究的 NMR 工具包在过去几十年中不断扩展,但它们往往仍然具有挑战性。在这里,我们表明,可溶性顺磁化合物 Gd(DTPA-BMA)引起的溶剂顺磁弛豫增强(sPRE)提供了 RNA 溶剂可及性的定量度量,并编码了与 RNA 结构相关的距离到表面信息,可提高 RNA 结构测定的准确性和收敛性。此外,我们表明,sPRE 数据可以很容易地从任何同位素标记方案的 RNA 中获得,并且在样品制备、稳定性和回收方面具有优势。sPRE 数据具有很大的动态范围,并反映了 RNA 的整体折叠,这表明它们非常适合于识别相互作用表面、评分结构模型以及作为 RNA 结构测定的约束条件。