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13C-direct 检测 NMR 实验用于 RNA 寡核苷酸的基于 J 偶合的顺序共振分配。

13C-direct detected NMR experiments for the sequential J-based resonance assignment of RNA oligonucleotides.

机构信息

Institute for Organic Chemistry and Chemical Biology, Johann Wolfgang Goethe-University Frankfurt, Frankfurt/M, Germany.

出版信息

J Biomol NMR. 2010 Aug;47(4):259-69. doi: 10.1007/s10858-010-9429-5. Epub 2010 Jun 11.

Abstract

We present here a set of (13)C-direct detected NMR experiments to facilitate the resonance assignment of RNA oligonucleotides. Three experiments have been developed: (1) the (H)CC-TOCSY-experiment utilizing a virtual decoupling scheme to assign the intraresidual ribose (13)C-spins, (2) the (H)CPC-experiment that correlates each phosphorus with the C4' nuclei of adjacent nucleotides via J(C,P) couplings and (3) the (H)CPC-CCH-TOCSY-experiment that correlates the phosphorus nuclei with the respective C1',H1' ribose signals. The experiments were applied to two RNA hairpin structures. The current set of (13)C-direct detected experiments allows direct and unambiguous assignment of the majority of the hetero nuclei and the identification of the individual ribose moieties following their sequential assignment. Thus, (13)C-direct detected NMR methods constitute useful complements to the conventional (1)H-detected approach for the resonance assignment of oligonucleotides that is often hindered by the limited chemical shift dispersion. The developed methods can also be applied to large deuterated RNAs.

摘要

我们在这里提出了一组(13)C 直接检测 NMR 实验,以方便 RNA 寡核苷酸的共振分配。已经开发了三个实验:(1)利用虚拟去耦方案分配残基内核糖(13)C 自旋的(H)CC-TOCSY 实验,(2)通过 J(C,P)偶联将每个磷与相邻核苷酸的 C4' 核相关联的(H)CPC 实验,以及(3)将磷核与各自的 C1',H1' 核糖信号相关联的(H)CPC-CCH-TOCSY 实验。这些实验应用于两种 RNA 发夹结构。当前的(13)C 直接检测实验集允许直接且明确地分配大多数杂核,并在进行顺序分配后识别各个核糖部分。因此,(13)C 直接检测 NMR 方法对于寡核苷酸的共振分配构成了对常规(1)H 检测方法的有用补充,后者通常受到有限的化学位移分散的阻碍。开发的方法也可以应用于大型氘化 RNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/364b/2900595/7aa7249fe7e4/10858_2010_9429_Fig1_HTML.jpg

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