Protein-Nucleic Acid Interaction Section, Structural Biophysics Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
Methods. 2010 Oct;52(2):180-91. doi: 10.1016/j.ymeth.2010.06.009. Epub 2010 Jun 8.
Among the greatest advances in biology today are the discoveries of various roles played by RNA in biological processes. However, despite significant advances in RNA structure determination using X-ray crystallography [1] and solution NMR [2-4], the number of bona fide RNA structures is very limited, in comparison with the growing number of known functional RNAs. This is because of great difficulty in growing crystals or/and obtaining phase information, and severe size constraints on structure determination by solution NMR spectroscopy. Clearly, there is an acute need for new methodologies for RNA structure determination. The prevailing approach for structure determination of RNA in solution is a "bottom-up" approach that was basically transplanted from the approach used for determining protein structures, despite vast differences in both structural features and chemical compositions between these two types of biomacromolecules. In this chapter, we describe a new method, which has been reported recently, for rapid global structure determination of RNAs using solution-based NMR spectroscopy and small-angle X-ray scattering. The method treats duplexes as major building blocks of RNA structures. By determining the global orientations of the duplexes and the overall shape, the global structure of an RNA can be constructed and further regularized using Xplor-NIH. The utility of the method was demonstrated in global structure determination of two RNAs, a 71-nt and 102-nt RNAs with an estimated backbone RMSD ∼3.0Å. The global structure opens door to high-resolution structure determination in solution.
在当今生物学领域的最大进展中,人们发现了 RNA 在生物过程中所扮演的各种角色。然而,尽管利用 X 射线晶体学[1]和溶液 NMR[2-4]在确定 RNA 结构方面取得了重大进展,但与越来越多已知功能的 RNA 相比,真正的 RNA 结构数量非常有限。这是因为晶体生长或/和获得相信息存在很大困难,并且溶液 NMR 光谱学在确定结构时受到严重的尺寸限制。显然,迫切需要新的 RNA 结构确定方法。在溶液中确定 RNA 结构的主要方法是一种“自下而上”的方法,该方法基本上是从用于确定蛋白质结构的方法移植而来的,尽管这两种生物大分子在结构特征和化学组成方面存在巨大差异。在本章中,我们描述了一种新方法,该方法最近已被报道,用于使用基于溶液的 NMR 光谱学和小角 X 射线散射快速确定 RNA 的整体结构。该方法将双链体视为 RNA 结构的主要构建块。通过确定双链体的全局取向和整体形状,可以构建 RNA 的全局结构,并使用 Xplor-NIH 对其进行进一步正则化。该方法的实用性已在两个 RNA(一个 71nt 和一个 102nt RNA)的全局结构确定中得到了证明,其估计的骨架 RMSD 约为 3.0Å。全局结构为在溶液中进行高分辨率结构确定打开了大门。