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A Novel Paramagnetic Relaxation Enhancement Tag forNucleic Acids: A Tool to Study Structure and Dynamics of RNA

机译:一种新型的顺磁弛豫增强标签核酸:研究RNA结构和动力学的工具

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摘要

In this work, we present a novel 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) radical phosphoramidite building block, which can be attached to the 5′-terminus of nucleic acids. To investigate the paramagnetic relaxation enhancement (PRE) emanating from this radical center, we incorporated the TEMPO label into various types of RNAs. We measured proton PREs for selectively 13C-isotope labeled nucleotides to derive long-range distance restraints in a short 15 nucleotide stem–loop model system, underscoring the potential of the 5′-TEMPO tag to determine long-range distance restraints for solution structure determination. We subsequently applied the distance-dependent relaxation enhancement induced by the nitroxide radical to discern two folding states in a bistable RNA. Finally, we investigated the fast conformational sampling of the HIV-1 TAR RNA, a paradigm for structural flexibility in nucleic acids. With PRE NMR in combination with molecular dynamics simulations, the structural plasticity of this RNA was analyzed in the absence and presence ofthe ligand l-argininamide.
机译:在这项工作中,我们提出了一种新型的2,2,6,6-四甲基哌啶1-氧基(TEMPO)自由基亚磷酰胺构件,该构件可以连接至核酸的5'-末端。为了研究从这个自由基中心发出的顺磁弛豫增强(PRE),我们将TEMPO标签整合到各种类型的RNA中。我们测量了质子PREs选择性地标记了 13 C同位素的核苷酸,以在短的15个核苷酸茎-环模型系统中获得远距离限制,强调了5'-TEMPO标签确定长链的潜力距离限制用于解决方案结构确定。我们随后应用了由氮氧自由基引起的距离依赖性弛豫增强来识别双稳态RNA中的两个折叠状态。最后,我们研究了HIV-1 TAR RNA的快速构象采样,这是核酸结构柔性的范例。结合PRE NMR和分子动力学模拟,可以在不存在或不存在RNA的情况下分析该RNA的结构可塑性配体1-精氨酰胺。

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