T. C. Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, Maryland 21218, USA.
Acc Chem Res. 2011 Dec 20;44(12):1312-9. doi: 10.1021/ar2000474. Epub 2011 Jun 29.
Many RNAs do not directly code proteins but are nonetheless indispensable to cellular function. These strands fold into intricate three-dimensional shapes that are essential structures in protein synthesis, splicing, and many other processes of gene regulation and expression. A variety of biophysical and biochemical methods are now showing, in real time, how ribosomal subunits and other ribonucleoprotein complexes assemble from their molecular components. Footprinting methods are particularly useful for studying the folding of long RNAs: they provide quantitative information about the conformational state of each residue and require little material. Data from footprinting complement the global information available from small-angle X-ray scattering or cryo-electron microscopy, as well as the dynamic information derived from single-molecule Förster resonance energy transfer (FRET) and NMR methods. In this Account, I discuss how we have used hydroxyl radical footprinting and other experimental methods to study pathways of RNA folding and 30S ribosome assembly. Hydroxyl radical footprinting probes the solvent accessibility of the RNA backbone at each residue in as little as 10 ms, providing detailed views of RNA folding pathways in real time. In conjunction with other methods such as solution scattering and single-molecule FRET, time-resolved footprinting of ribozymes showed that stable domains of RNA tertiary structure fold in less than 1 s. However, the free energy landscapes for RNA folding are rugged, and individual molecules kinetically partition into folding pathways that lead through metastable intermediates, stalling the folding or assembly process. Time-resolved footprinting was used to follow the formation of tertiary structure and protein interactions in the 16S ribosomal RNA (rRNA) during the assembly of 30S ribosomes. As previously observed in much simpler ribozymes, assembly occurs in stages, with individual molecules taking different routes to the final complex. Interactions occur concurrently in all domains of the 16S rRNA, and multistage protection of binding sites of individual proteins suggests that initial encounter complexes between the rRNA and ribosomal proteins are remodeled during assembly. Equilibrium footprinting experiments showed that one primary binding protein was sufficient to stabilize the tertiary structure of the entire 16S 5'-domain. The rich detail available from the footprinting data showed that the secondary assembly protein S16 suppresses non-native structures in the 16S 5'-domain. In doing so, S16 enables a conformational switch distant from its own binding site, which may play a role in establishing interactions with other domains of the 30S subunit. Together, the footprinting results show how protein-induced changes in RNA structure are communicated over long distances, ensuring cooperative assembly of even very large RNA-protein complexes such as the ribosome.
许多 RNA 并不直接编码蛋白质,但对细胞功能却不可或缺。这些 RNA 链折叠成复杂的三维形状,是蛋白质合成、剪接和许多其他基因调控和表达过程的重要结构。现在,各种生物物理和生化方法正在实时展示核糖体亚基和其他核糖核蛋白复合物如何从其分子成分组装而成。足迹法特别适用于研究长 RNA 的折叠:它们提供了关于每个残基构象状态的定量信息,并且需要的材料很少。足迹法的数据补充了小角度 X 射线散射或低温电子显微镜提供的全局信息,以及来自单分子Förster 共振能量转移(FRET)和 NMR 方法的动态信息。在本报告中,我讨论了我们如何使用羟基自由基足迹法和其他实验方法来研究 RNA 折叠和 30S 核糖体组装的途径。羟基自由基足迹法在短短 10 毫秒内探测到每个残基 RNA 骨架的溶剂可及性,实时提供 RNA 折叠途径的详细视图。与其他方法(如溶液散射和单分子 FRET)结合使用时,核酶的时间分辨足迹表明,RNA 三级结构的稳定结构域在不到 1 秒内折叠。然而,RNA 折叠的自由能景观崎岖不平,单个分子在动力学上分配到导致亚稳态中间体的折叠途径中,从而使折叠或组装过程停滞。时间分辨足迹法用于研究在 30S 核糖体组装过程中 16S 核糖体 RNA(rRNA)形成三级结构和蛋白质相互作用的过程。如在更简单的核酶中先前观察到的那样,组装分阶段进行,单个分子采用不同的途径到达最终复合物。各个结构域中的相互作用同时发生,单个蛋白质的结合位点的多阶段保护表明,rRNA 和核糖体蛋白之间的初始相遇复合物在组装过程中被重塑。平衡足迹实验表明,一个主要的结合蛋白足以稳定整个 16S 5'-结构域的三级结构。足迹数据提供的丰富细节表明,二级组装蛋白 S16 抑制 16S 5'-结构域中的非天然结构。通过这样做,S16 使远离其自身结合位点的构象转换成为可能,这可能在与 30S 亚基的其他结构域建立相互作用中发挥作用。总之,足迹法结果表明,蛋白质诱导的 RNA 结构变化如何在长距离内传递,确保即使是非常大的 RNA-蛋白质复合物(如核糖体)的协同组装。