基于核磁共振波谱和MD模拟的SARS-CoV-2三角洲s2m根茎环结构异质性和动力学研究

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Maria A Wirtz Martin, Joseph A Makowski, Tobias Matzel, Adam H Kensinger, Alexander Herr, Christian Richter, Hendrik R A Jonker, Anna Wacker, Jeffrey D Evanseck, Harald Schwalbe
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引用次数: 0

摘要

在结构化rna中,螺旋元件通常被顶端环覆盖,顶端环是完整的结构元件,平均大小从3到20吨不等,并且显示出高度异质性的能量景观剖面,这使得结构表征特别具有挑战性。本文采用核磁共振波谱(NMR)、小角x射线散射(SAXS)和分子动力学模拟(MD)的综合方法,对含有高动态非环路的SARS-CoV-2 Delta s2m元素进行了表征。我们进一步探索了s2m非环路及其瞬时闭合5 ‘ -G-U-3 ’碱基对的构象空间,通过实验核磁共振观测值加权的MD模拟,得到了s2m非环路基序的全面表征。我们将集成反卷积到构象和动力学中,为未来具有动态基序的RNA结构的集成功能表征提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural heterogeneity and dynamics in the apical stem loop of s2m from SARS-CoV-2 Delta by an integrative NMR spectroscopy and MD simulation approach
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.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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