Wirtz Martin Maria A, Makowski Joseph A, Matzel Tobias, Kensinger Adam H, Herr Alexander, Richter Christian, Jonker Hendrik R A, Wacker Anna, Evanseck Jeffrey D, Schwalbe Harald
Institute for Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance (BMRZ), Goethe University Frankfurt, Max-von-Laue-Str. 7, 60438 Frankfurt, Germany.
Department of Chemistry and Biochemistry and Center for Computational Sciences, Duquesne University, Pittsburgh, PA 15282, United States.
Nucleic Acids Res. 2025 Jun 20;53(12). doi: 10.1093/nar/gkaf552.
In structured RNAs, helical elements are often capped by apical loops that are integral structural elements, ranging from 3 to >20 nts of size on average, and display a highly heterogeneous energy landscape profile, rendering structural characterization particularly challenging. We here provide a characterization of the SARS-CoV-2 Delta s2m element containing a highly dynamic nonaloop using an integrative approach of nuclear magnetic resonance spectroscopy (NMR), small angle X-ray scattering (SAXS), and molecular dynamics simulations (MD). We further explored the conformational space in the s2m nonaloop and its transient closing 5'-G-U-3' base pair by MD simulations weighted by experimental NMR observables, leading to a comprehensive representation of the s2m nonaloop motif. Our deconvolution of the ensemble into conformations and dynamics provides a basis for future ensemble-functional characterization of RNA structures featuring dynamic motifs.
在结构化RNA中,螺旋元件通常由顶端环封端,这些顶端环是不可或缺的结构元件,平均大小从3个核苷酸到超过20个核苷酸不等,并且呈现出高度异质的能量景观分布,这使得结构表征极具挑战性。我们在此使用核磁共振光谱(NMR)、小角X射线散射(SAXS)和分子动力学模拟(MD)的综合方法,对包含高度动态非环的SARS-CoV-2 Delta s2m元件进行了表征。我们通过由实验NMR可观测量加权的MD模拟,进一步探索了s2m非环及其瞬时闭合的5'-G-U-3'碱基对中的构象空间,从而全面呈现了s2m非环基序。我们将集合解卷积为构象和动力学,为未来对具有动态基序的RNA结构进行集合功能表征奠定了基础。