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对越来越大的RNA进行氮检测氢-氮相关实验的评估。

Evaluation of N-detected H-N correlation experiments on increasingly large RNAs.

作者信息

Schnieders Robbin, Richter Christian, Warhaut Sven, de Jesus Vanessa, Keyhani Sara, Duchardt-Ferner Elke, Keller Heiko, Wöhnert Jens, Kuhn Lars T, Breeze Alexander L, Bermel Wolfgang, Schwalbe Harald, Fürtig Boris

机构信息

Institute for Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance (BMRZ), Johann Wolfgang Goethe-Universität Frankfurt, Max-von-Laue-Str. 7, 60438, Frankfurt, Germany.

Institute for Molecular Biosciences, Center for Biomolecular Magnetic Resonance (BMRZ), Johann Wolfgang Goethe-Universität Frankfurt, Max-von-Laue Str. 9, 60438, Frankfurt, Germany.

出版信息

J Biomol NMR. 2017 Sep;69(1):31-44. doi: 10.1007/s10858-017-0132-7. Epub 2017 Sep 6.

DOI:10.1007/s10858-017-0132-7
PMID:28879611
Abstract

Recently, N-detected multidimensional NMR experiments have been introduced for the investigation of proteins. Utilization of the slow transverse relaxation of nitrogen nuclei in a N-TROSY experiment allowed recording of high quality spectra for high molecular weight proteins, even in the absence of deuteration. Here, we demonstrate the applicability of three N-detected H-N correlation experiments (TROSY, BEST-TROSY and HSQC) to RNA. With the newly established N-detected BEST-TROSY experiment, which proves to be the most sensitive N-detected H-N correlation experiment, spectra for five RNA molecules ranging in size from 5 to 100 kDa were recorded. These spectra yielded high resolution in the N-dimension even for larger RNAs since the increase in line width with molecular weight is more pronounced in the H- than in the N-dimension. Further, we could experimentally validate the difference in relaxation behavior of imino groups in AU and GC base pairs. Additionally, we showed that N-detected experiments theoretically should benefit from sensitivity and resolution advantages at higher static fields but that the latter is obscured by exchange dynamics within the RNAs.

摘要

最近,已引入检测氮的多维核磁共振实验来研究蛋白质。在N-TROSY实验中利用氮核的缓慢横向弛豫,即使在没有氘代的情况下,也能为高分子量蛋白质记录高质量的光谱。在此,我们证明了三种检测氮的氢-氮相关实验(TROSY、BEST-TROSY和HSQC)对RNA的适用性。新建立的检测氮的BEST-TROSY实验被证明是最灵敏的检测氮的氢-氮相关实验,记录了大小从5到100 kDa的五个RNA分子的光谱。这些光谱即使对于较大的RNA在氮维度上也产生了高分辨率,因为线宽随分子量的增加在氢维度上比在氮维度上更明显。此外,我们可以通过实验验证AU和GC碱基对中亚氨基基团弛豫行为的差异。另外,我们表明检测氮的实验理论上应在更高静磁场下受益于灵敏度和分辨率优势,但后者被RNA内的交换动力学所掩盖。

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Perspective: revisiting the field dependence of TROSY sensitivity.观点:重新审视横向弛豫优化谱(TROSY)灵敏度的场依赖性。
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An accurately preorganized IRES RNA structure enables eIF4G capture for initiation of viral translation.精确预组织的内部核糖体进入位点(IRES)RNA结构能够捕获真核翻译起始因子4G(eIF4G)以启动病毒翻译。
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F NMR-Based Fragment Screening for 14 Different Biologically Active RNAs and 10 DNA and Protein Counter-Screens.基于 14 种不同生物活性 RNA 的 F NMR 片段筛选及 10 种 DNA 和蛋白质对照筛选。
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More than Proton Detection-New Avenues for NMR Spectroscopy of RNA.超越质子探测——RNA 的 NMR 光谱学新途径。
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