Laboratory of Organic Chemistry , Wageningen University , Stippeneng 4 , 6708 WE Wageningen , The Netherlands.
TI-COAST , Science Park 904 , 1098 XH Amsterdam , The Netherlands.
J Am Soc Mass Spectrom. 2020 Feb 5;31(2):249-256. doi: 10.1021/jasms.9b00082. Epub 2020 Jan 8.
Identification and confirmation of known as well as unknown (bio)chemical entities in ambient mass spectrometry (MS) and MS imaging (MSI) mostly involve accurate mass determination, often in combination with MS/MS or MS work flows. To further improve structural assignment, additional molecular information is required. Here we present an ambient hydrogen/deuterium exchange (HDX) laser ablation electrospray ionization (LAESI) MS method in which, apart from the accurate mass and MS/MS data, the number of exchangeable protons in (un)known molecules is obtained. While eventually presenting ambient HDX-LAESI-MSI, samples were not preincubated with deuterated solvents, but instead HDX occurred following fusion of ablated sample material with microdroplets generated by ESI of deuterated solvents. Therefore, the degree of HDX was first studied following ablation of nondeuterated sample solutions of melamine and monosaccharides. From these experiments, it was concluded that the set-up used could provide meaningful HDX data in support of molecular structure elucidation by significantly reducing the number of structure options from a measured elemental composition. This reduction was demonstrated with an unknown accurate value obtained in the analysis of an orange slice, reducing the possible number of molecular structures having the same elemental composition by 87% due to the number of H/D exchanges observed. Next, deuterated and nondeuterated MS/MS experiments showed the number of exchangeable protons in the substructures from deuterated neutral losses in the product ion spectra, confirming the compound to be arginine. Finally, the potential of ambient HDX-LAESI-MSI was demonstrated by the imaging of (secondary) plant metabolites in a petal.
在环境质谱(MS)和 MS 成像(MSI)中,识别和确认已知和未知(生物)化学实体主要涉及准确质量测定,通常结合 MS/MS 或 MS 工作流程。为了进一步提高结构分配,需要额外的分子信息。在这里,我们提出了一种环境氢/氘交换(HDX)激光烧蚀电喷雾电离(LAESI)MS 方法,其中除了准确的质量和 MS/MS 数据外,还可以获得(未)知分子中的可交换质子数。虽然最终提出了环境 HDX-LAESI-MSI,但样品没有用氘化溶剂预孵育,而是在烧蚀的样品材料与由氘化溶剂的 ESI 产生的微滴融合后发生 HDX。因此,首先研究了非氘化样品溶液中三聚氰胺和单糖的烧蚀后 HDX 的程度。从这些实验中得出结论,所使用的装置可以通过大大减少从测量的元素组成得出的分子结构选项的数量,提供有意义的 HDX 数据,以支持分子结构阐明。这通过在分析橙色切片时获得的未知准确 值得到了证明,由于观察到的 H/D 交换数量,具有相同元素组成的分子结构的可能数量减少了 87%。接下来,氘化和非氘化 MS/MS 实验显示了从产物离子谱中氘化中性损失的亚结构中可交换质子的数量,从而证实该化合物为精氨酸。最后,通过在花瓣中成像(次级)植物代谢物,证明了环境 HDX-LAESI-MSI 的潜力。