Carbohydrates have a wide variety of structures whose complexity and heterogeneity challenge the field of analytical chemistry. Tandem mass spectrometry, with its remarkable sensitivity and high information content, provides key advantages to addressing the structural elucidation of polysaccharides. Yet, classical fragmentation by collision-activated dissociation (CAD) in many cases fails to reach a comprehensive structural determination, especially when isomers have to be differentiated. In this work, for the first time, vacuum ultra-violet (VUV) synchrotron radiation is used as the activation process in tandem mass spectrometry of large oligosaccharides. Compared to low energy CAD (LE-CAD), photon activated dissociation brought more straightforward and valuable structural information. The outstanding feature was that complete series of informative ions were produced, with only minor neutral losses. Moreover, systematic fragmentation rules could be drawn thus facilitating the definitive assignments of fragment identities. As a result, most of the structures present in a complex mixture of oligogalacturonans could be comprehensively resolved, including many isomers differing in the position of methyl groups along the galacturonic acid backbone.
Keywords: CAD; DM; DPI; ECD; EDD; EID; ESI; ETD; HE; HILIC; HPAEC; Hhigh-energy; IC; IP; IVR; Isomers; LE; MALDI; MS; Oligogalacturonans; PD; PGC; RP; SEC; Structure; TOF; Tandem mass spectrometry; UHPLC; VUV; Vacuum ultra-violet synchrotron photon activation; collision activated dissociation; degree of methylation; dissociative photoionization; electron capture dissociation; electron detachment dissociation; electron induced dissociation; electron transfer dissociation; electrospray ionization; high-performance anionic exchange chromatography; hydrophilic interaction liquid chromatography; internal conversion; internal vibrational redistribution; ion pairing; low-energy; mass spectrometry; matrix assisted laser desorption ionization; photo-dissociation; porous graphitized carbon; reverse-phase; size exclusion chromatography; time of flight; ultra-high performance liquid chromatography; vacuum ultra-violet.
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