首页> 外文期刊>Journal of Biomolecular NMR >Application of iterative soft thresholding for fast reconstruction of NMR data non-uniformly sampled with multidimensional Poisson Gap scheduling
【24h】

Application of iterative soft thresholding for fast reconstruction of NMR data non-uniformly sampled with multidimensional Poisson Gap scheduling

机译:迭代软阈值技术在多维Poisson Gap调度非均匀采样的NMR数据快速重建中的应用

获取原文
获取原文并翻译 | 示例
           

摘要

The fast Fourier transformation has been the gold standard for transforming data from time to frequency domain in many spectroscopic methods, including NMR. While reliable, it has as a drawback that it requires a grid of uniformly sampled data points. This needs very long measuring times for sampling in multidimensional experiments in all indirect dimensions uniformly and even does not allow reaching optimal evolution times that would match the resolution power of modern high-field instruments. Thus, many alternative sampling and transformation schemes have been proposed. Their common challenges are the suppression of the artifacts due to the non-uniformity of the sampling schedules, the preservation of the relative signal amplitudes, and the computing time needed for spectra reconstruction. Here we present a fast implementation of the Iterative Soft Thresholding approach (istHMS) that can reconstruct highresolution non-uniformly sampled NMR data up to four dimensions within a few hours and make routine reconstruction of high-resolution NUS 3D and 4D spectra convenient. We include a graphical user interface for generating sampling schedules with the Poisson-Gap method and an estimation of optimal evolution times based on molecular properties. The performance of the approach is demonstrated with the reconstruction of non-uniformly sampled medium and high-resolution 3D and 4D protein spectra acquired with sampling densities as low as 0.8%. The method presented here facilitates acquisition, reconstruction and use of multidimensional NMR spectra at otherwise unreachable spectral resolution in indirect dimensions.
机译:快速傅立叶变换已成为在包括NMR在内的许多光谱方法中将数据从时域转换到频域的黄金标准。虽然可靠,但它的缺点是需要一个均匀采样的数据点的网格。这需要非常长的测量时间才能在所有间接维度上统一进行多维实验采样,甚至不允许达到与现代高场仪器的分辨率能力相匹配的最佳演化时间。因此,已经提出了许多替代的采样和变换方案。它们共同的挑战是由于采样时间表的不均匀而导致的伪影抑制,相对信号幅度的保留以及频谱重建所需的计算时间。在这里,我们介绍了迭代软阈值方法(istHMS)的快速实现,该方法可以在几个小时内将高分辨率非均匀采样的NMR数据重构为四个维度,并使高分辨率NUS 3D和4D光谱的常规重构变得方便。我们包括一个图形用户界面,用于使用Poisson-Gap方法生成采样计划,并根据分子特性估算最佳进化时间。通过重建非均匀采样的介质以及以低至0.8%的采样密度获取的高分辨率3D和4D蛋白光谱,可以证明该方法的性能。此处介绍的方法有助于获取,重建和使用多维NMR光谱,这些光谱在间接维度上无法达到光谱分辨率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号