Department of Chemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
Nucleic Acids Res. 2024 Jul 22;52(13):e59. doi: 10.1093/nar/gkae496.
The functional diversity of RNAs is encoded in their innate conformational heterogeneity. The combination of single-molecule spectroscopy and computational modeling offers new attractive opportunities to map structural transitions within nucleic acid ensembles. Here, we describe a framework to harmonize single-molecule Förster resonance energy transfer (FRET) measurements with molecular dynamics simulations and de novo structure prediction. Using either all-atom or implicit fluorophore modeling, we recreate FRET experiments in silico, visualize the underlying structural dynamics and quantify the reaction coordinates. Using multiple accessible-contact volumes as a post hoc scoring method for fragment assembly in Rosetta, we demonstrate that FRET can be used to filter a de novo RNA structure prediction ensemble by refuting models that are not compatible with in vitro FRET measurement. We benchmark our FRET-assisted modeling approach on double-labeled DNA strands and validate it against an intrinsically dynamic manganese(II)-binding riboswitch. We show that a FRET coordinate describing the assembly of a four-way junction allows our pipeline to recapitulate the global fold of the riboswitch displayed by the crystal structure. We conclude that computational fluorescence spectroscopy facilitates the interpretability of dynamic structural ensembles and improves the mechanistic understanding of nucleic acid interactions.
RNA 的功能多样性被编码在其固有的构象异质性中。单分子光谱学和计算建模的结合为绘制核酸集合内的结构转变提供了新的有吸引力的机会。在这里,我们描述了一种将单分子Förster 共振能量转移 (FRET) 测量与分子动力学模拟和从头预测结构相结合的框架。使用全原子或隐式荧光团建模,我们在计算机上重现 FRET 实验,可视化潜在的结构动力学并量化反应坐标。使用多个可访问接触体积作为 Rosetta 中片段组装的事后评分方法,我们证明 FRET 可用于通过反驳与体外 FRET 测量不兼容的模型来过滤从头 RNA 结构预测集合。我们在双链 DNA 上对我们的 FRET 辅助建模方法进行了基准测试,并通过内在动态锰 (II) 结合核酶对其进行了验证。我们表明,描述四联体组装的 FRET 坐标允许我们的流水线重现晶体结构显示的核酶的全局折叠。我们得出结论,计算荧光光谱学促进了动态结构集合的可解释性,并提高了对核酸相互作用的机制理解。