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High-Resolution Iterative Frequency Identification for NMR as a General Strategy for Multidimensional Data Collection

机译:NMR的高分辨率迭代频率识别作为多维数据收集的一般策略

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We describe a novel approach to the rapid collection and processing of multidimensional NMR data: "high-resolution iterative frequency identification for NMR" (HIFI-NMR). As with other reduced dimensionality approaches, HIFI-NMR collects n-dimensional data as a set of two-dimensional (2D) planes. The HIFI-NMR algorithm incorporates several innovative features. (1) Following the initial collection of two orthogonal 2D planes, tilted planes are selected adaptively, one-by-one. (2) Spectral space is analyzed in a rigorous statistical manner. (3) An online algorithm maintains a model that provides a probabilistic representation of the three-dimensional (3D) peak positions, derives the optimal angle for the next plane to be collected, and stops data collection when the addition of another plane would not improve the data model. (4) A robust statistical algorithm extracts information from the plane projections and is used to drive data collection. (5) Peak lists with associated probabilities are generated directly, without total reconstruction of the 3D spectrum; these are ready for use in subsequent assignment or structure determination steps. As a proof of principle, we have tested the approach with 3D triple-resonance experiments of the kind used to assign protein backbone and side-chain resonances. Peaks extracted automatically by HIFI-NMR, for both small and larger proteins, included ~98% of real peaks obtained from control experiments in which data were collected by conventional 3D methods. HIFI-NMR required about one-tenth the time for data collection and avoided subsequent data processing and peak-picking. The approach can be implemented on commercial NMR spectrometers and is extensible to higher-dimensional NMR.
机译:我们描述了一种快速收集和处理多维NMR数据的新颖方法:“用于NMR的高分辨率迭代频率识别”(HIFI-NMR)。与其他降维方法一样,HIFI-NMR收集n维数据作为一组二维(2D)平面。 HIFI-NMR算法具有多项创新功能。 (1)在最初收集两个正交的2D平面之后,以一对一的方式自适应地选择倾斜的平面。 (2)以严格的统计方式分析光谱空间。 (3)一种在线算法维护着一个模型,该模型提供了三维(3D)峰位置的概率表示,得出了要收集的下一个平面的最佳角度,并在添加另一个平面不会改善时停止数据收集数据模型。 (4)鲁棒的统计算法从平面投影中提取信息,并用于驱动数据收集。 (5)直接生成具有相关概率的峰列表,而无需完全重建3D频谱;这些都可以在后续的分配或结构确定步骤中使用。作为原理的证明,我们已经用3D三重共振实验对这种方法进行了测试,这种实验用于分配蛋白质骨架和侧链共振。通过HIFI-NMR自动提取的大小蛋白质的峰,包括从对照实验中获得的真实峰的约98%,在该实验中,常规3D方法收集了数据。 HIFI-NMR大约需要数据收集时间的十分之一,并且避免了后续的数据处理和峰采集。该方法可以在商用NMR光谱仪上实现,并且可以扩展到更高维度的NMR。

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