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Improved NMR Detection of Phospho-Metabolites in a Complex Mixture

机译:改进了复杂混合物中磷代代谢物的NMR检测

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Phosphorylated metabolites are omnipresent in cells, but their analytical characterization faces several technical hurdles. Here, we detail an improved NMR workflow aimed at assigning the high-resolution subspectrum of the phospho-metabolites in a complex mixture. Combining a pure absorption J -resolved spectrum ( Pell, A. J. ; J. Magn. Reson. 2007, 189 (2), 293?299) with alternate on- and off-switching of the ~(31)P coupling interaction during the t _(1) evolution with a pure in-phase (PIP) HSQMBC experiment ( Casta?ar, L. ; Angew. Chem., Int. Ed. 2014, 53 (32), 8379?8382) without or with total correlation spectroscopy (TOCSY) transfer during the insensitive nuclei enhancement by polarization transfer (INEPT) gives access to selective identification of the individual subspectra of the phosphorylated metabolites. Returning to the initial J -res spectra, we can extract with optimal resolution the full trace for the individual phospho-metabolites, which can then be transposed on the high-resolution quantitative one dimensional spectrum.
机译:磷酸化代谢物在细胞中无处不在,但其分析表征面临几个技术障碍。在这里,我们详细介绍了一种改进的核磁共振工作流程,旨在分配复杂混合物中磷酸代谢物的高分辨率子光谱。结合纯吸收J-分辨光谱(Pell,a.J.;J.Magn.Reson.2007,189(2),293?299)通过纯同相(PIP)HSQMBC实验(Casta?ar,L.;Angew.Chem.,Int.Ed.2014,53(32),8379?)在t_1)演化过程中交替开启和关闭~(31)P耦合相互作用?8382)在不敏感核的极化增强过程中,不使用或使用总相关光谱(TOCSY)转移(INEPT)可以选择性地识别磷酸化代谢物的单个亚谱。回到初始J-res光谱,我们可以以最佳分辨率提取单个磷酸代谢物的完整痕迹,然后将其转置到高分辨率定量一维光谱上。

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