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RNA-PAIRS:RNA 亚甲基质子位移的概率赋值。

RNA-PAIRS: RNA probabilistic assignment of imino resonance shifts.

机构信息

National Magnetic Resonance Facility at Madison, Madison, WI, USA.

出版信息

J Biomol NMR. 2012 Apr;52(4):289-302. doi: 10.1007/s10858-012-9603-z. Epub 2012 Feb 23.

Abstract

The significant biological role of RNA has further highlighted the need for improving the accuracy, efficiency and the reach of methods for investigating RNA structure and function. Nuclear magnetic resonance (NMR) spectroscopy is vital to furthering the goals of RNA structural biology because of its distinctive capabilities. However, the dispersion pattern in the NMR spectra of RNA makes automated resonance assignment, a key step in NMR investigation of biomolecules, remarkably challenging. Herein we present RNA Probabilistic Assignment of Imino Resonance Shifts (RNA-PAIRS), a method for the automated assignment of RNA imino resonances with synchronized verification and correction of predicted secondary structure. RNA-PAIRS represents an advance in modeling the assignment paradigm because it seeds the probabilistic network for assignment with experimental NMR data, and predicted RNA secondary structure, simultaneously and from the start. Subsequently, RNA-PAIRS sets in motion a dynamic network that reverberates between predictions and experimental evidence in order to reconcile and rectify resonance assignments and secondary structure information. The procedure is halted when assignments and base-parings are deemed to be most consistent with observed crosspeaks. The current implementation of RNA-PAIRS uses an initial peak list derived from proton-nitrogen heteronuclear multiple quantum correlation ((1)H-(15)N 2D HMQC) and proton-proton nuclear Overhauser enhancement spectroscopy ((1)H-(1)H 2D NOESY) experiments. We have evaluated the performance of RNA-PAIRS by using it to analyze NMR datasets from 26 previously studied RNAs, including a 111-nucleotide complex. For moderately sized RNA molecules, and over a range of comparatively complex structural motifs, the average assignment accuracy exceeds 90%, while the average base pair prediction accuracy exceeded 93%. RNA-PAIRS yielded accurate assignments and base pairings consistent with imino resonances for a majority of the NMR resonances, even when the initial predictions are only modestly accurate. RNA-PAIRS is available as a public web-server at http://pine.nmrfam.wisc.edu/RNA/.

摘要

RNA 的重要生物学作用进一步凸显了提高研究 RNA 结构和功能的方法的准确性、效率和广度的必要性。由于其独特的能力,核磁共振(NMR)光谱对于推进 RNA 结构生物学的目标至关重要。然而,RNA 的 NMR 光谱中的频散模式使得自动共振分配,即 NMR 研究生物分子的关键步骤,变得极具挑战性。在这里,我们提出了 RNA 亚氨基共振位移的概率分配(RNA-PAIRS),这是一种自动分配 RNA 亚氨基共振的方法,同时同步验证和校正预测的二级结构。RNA-PAIRS 代表了分配范式建模方面的一项进展,因为它使用实验 NMR 数据和预测的 RNA 二级结构同时且从一开始就为分配概率网络播种。随后,RNA-PAIRS 启动了一个动态网络,在预测和实验证据之间来回传递,以协调和纠正共振分配和二级结构信息。当分配和碱基配对被认为与观察到的交叉峰最一致时,该过程就会停止。RNA-PAIRS 的当前实现使用源自质子-氮异核多维相关((1)H-(15)N 2D HMQC)和质子-质子核 Overhauser 增强光谱((1)H-(1)H 2D NOESY)实验的初始峰列表。我们通过使用它来分析来自 26 个先前研究过的 RNA 的 NMR 数据集,包括一个 111 个核苷酸的复合物,来评估 RNA-PAIRS 的性能。对于中等大小的 RNA 分子,并且在一系列相对复杂的结构模体中,平均分配准确率超过 90%,而平均碱基对预测准确率超过 93%。即使初始预测仅略有准确,RNA-PAIRS 也能为大多数 NMR 共振产生与亚氨基共振一致的准确分配和碱基配对。RNA-PAIRS 可在 http://pine.nmrfam.wisc.edu/RNA/ 作为公共网络服务器使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/3480180/accb32f611bc/nihms410283f1.jpg

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