Cox Neil, Millard Pierre, Charlier Cyril, Lippens Guy
TBI, Université de Toulouse, CNRS, INRAE, INSA, 31077 Toulouse, France.
Anal Chem. 2021 Mar 23;93(11):4818-4824. doi: 10.1021/acs.analchem.0c04056. Epub 2021 Mar 12.
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 -resolved spectrum (Pell, A. J.; 2007, 189 (2), 293-299) with alternate on- and off-switching of the P coupling interaction during the evolution with a pure in-phase (PIP) HSQMBC experiment (Castañar, L.; 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 -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.
磷酸化代谢物在细胞中普遍存在,但其分析表征面临若干技术障碍。在此,我们详细介绍一种改进的核磁共振工作流程,旨在确定复杂混合物中磷酸化代谢物的高分辨率子光谱。将纯吸收分辨光谱(Pell, A. J.; 2007, 189 (2), 293 - 299)与在演化过程中交替开启和关闭P耦合相互作用,并结合纯同相(PIP)HSQMBC实验(Castañar, L.; 2014, 53 (32), 8379 - 8382),在通过极化转移增强非灵敏核(INEPT)期间有无全相关谱(TOCSY)转移,从而能够选择性地识别磷酸化代谢物的各个子光谱。回到初始分辨光谱,我们可以以最佳分辨率提取各个磷酸化代谢物的完整轨迹,然后将其转换到高分辨率定量一维光谱上。