Spalding Jonathan L, Cho Kevin, Mahieu Nathaniel G, Nikolskiy Igor, Llufrio Elizabeth M, Johnson Stephen L, Patti Gary J
Department of Chemistry, Washington University in St. Louis , St. Louis, Missouri 63130, United States.
Department of Genetics, Washington University School of Medicine , St. Louis, Missouri 63110, United States.
Anal Chem. 2016 Mar 1;88(5):2538-42. doi: 10.1021/acs.analchem.5b04925. Epub 2016 Feb 11.
Metabolite identifications are most frequently achieved in untargeted metabolomics by matching precursor mass and full, high-resolution MS(2) spectra to metabolite databases and standards. Here we considered an alternative approach for establishing metabolite identifications that does not rely on full, high-resolution MS(2) spectra. First, we select mass-to-charge regions containing the most informative metabolite fragments and designate them as bins. We then translate each metabolite fragmentation pattern into a binary code by assigning 1's to bins containing fragments and 0's to bins without fragments. With 20 bins, this binary-code system is capable of distinguishing 96% of the compounds in the METLIN MS(2) library. A major advantage of the approach is that it extends untargeted metabolomics to low-resolution triple quadrupole (QqQ) instruments, which are typically less expensive and more robust than other types of mass spectrometers. We demonstrate a method of acquiring MS(2) data in which the third quadrupole of a QqQ instrument cycles over 20 wide isolation windows (coinciding with the location and width of our bins) for each precursor mass selected by the first quadrupole. Operating the QqQ instrument in this mode yields diagnostic bar codes for each precursor mass that can be matched to the bar codes of metabolite standards. Furthermore, our data suggest that using low-resolution bar codes enables QqQ instruments to make MS(2)-based identifications in untargeted metabolomics with a specificity and sensitivity that is competitive to high-resolution time-of-flight technologies.
在非靶向代谢组学中,代谢物鉴定最常见的方法是将前体质量以及完整的高分辨率二级质谱(MS(2))谱图与代谢物数据库和标准品进行匹配。在此,我们考虑了一种不依赖完整高分辨率MS(2)谱图来进行代谢物鉴定的替代方法。首先,我们选择包含最具信息性代谢物碎片的质荷比区域,并将其指定为区间。然后,我们通过为包含碎片的区间赋值1,为不包含碎片的区间赋值0,将每种代谢物的碎裂模式转换为二进制代码。对于20个区间,这种二进制代码系统能够区分METLIN二级质谱库中96%的化合物。该方法的一个主要优点是,它将非靶向代谢组学扩展到了低分辨率的三重四极杆(QqQ)仪器,这类仪器通常比其他类型的质谱仪更便宜且更耐用。我们展示了一种获取二级质谱数据的方法,即对于由第一重四极杆选择的每个前体质量,QqQ仪器的第三重四极杆在20个宽隔离窗口(与我们的区间位置和宽度一致)上循环。以这种模式操作QqQ仪器可为每个前体质量生成诊断条形码,这些条形码可与代谢物标准品的条形码进行匹配。此外,我们的数据表明,使用低分辨率条形码能使QqQ仪器在非靶向代谢组学中基于二级质谱进行鉴定,其特异性和灵敏度可与高分辨率飞行时间技术相媲美。