Selective deuteration of an RNA:RNA complex for structural analysis using small-angle scattering

Aldrex Munsayac, Wellington C Leite, Jesse B Hopkins, Ian Hall, Hugh M O'Neill, Sarah C Keane
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Abstract

The structures of RNA:RNA complexes regulate many biological processes. Despite their importance, protein-free RNA:RNA complexes represent a tiny fraction of experimentally-determined structures. Here, we describe a joint small-angle X-ray and neutron scattering (SAXS/SANS) approach to structurally interrogate conformational changes in a model RNA:RNA complex. Using SAXS, we measured the solution structures of the individual RNAs in their free state and of the overall RNA:RNA complex. With SANS, we demonstrate, as a proof-of-principle, that isotope labeling and contrast matching (CM) can be combined to probe the bound state structure of an RNA within a selectively deuterated RNA:RNA complex. Furthermore, we show that experimental scattering data can validate and improve predicted AlphaFold 3 RNA:RNA complex structures to reflect its solution structure. Our work demonstrates that in silico modeling, SAXS, and CM-SANS can be used in concert to directly analyze conformational changes within RNAs when in complex, enhancing our understanding of RNA structure in functional assemblies.
利用小角散射对 RNA:RNA 复合物进行选择性氘化以进行结构分析
RNA:RNA 复合物的结构调控着许多生物过程。尽管它们非常重要,但不含蛋白质的 RNA:RNA 复合物只占实验确定结构的极小一部分。在这里,我们介绍了一种联合小角 X 射线和中子散射(SAXS/SANS)方法,从结构上分析模型 RNA:RNA 复合物的构象变化。利用 SAXS,我们测量了自由状态下单个 RNA 和整个 RNA:RNA 复合物的溶液结构。作为原理验证,我们利用 SANS 证明了同位素标记和对比度匹配 (CM) 可以结合起来探测选择性氚化 RNA:RNA 复合物中 RNA 的结合态结构。此外,我们还展示了实验散射数据可以验证和改进预测的 AlphaFold 3 RNA:RNA 复合物结构,以反映其溶液结构。我们的工作表明,硅建模、SAXS 和 CM-SANS 可以协同使用,直接分析 RNA 在复合物中的构象变化,从而增强我们对功能组装中 RNA 结构的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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