Structure Determination of Large Isomeric Oligosaccharides of Natural Origin through Multipass and Multistage Cyclic Traveling-Wave Ion Mobility Mass Spectrometry

• Published in: Analytical chemistry (Washington) Vol. 91; no. 18; pp. 12030 - 12037
• Main Authors: Ropartz, David, Fanuel, Mathieu, Ujma, Jakub, Palmer, Martin, Giles, Kevin, Rogniaux, Hélène
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 17.09.2019
• Subjects: Abundance; Analytical chemistry; Atomic properties; Carbohydrates; Cell walls; Chemistry; Conformation; Ionic mobility; Ions; Isomers; Life Sciences; Mass spectrometry; Mass spectroscopy; Mobility; Oligosaccharides; Quadrupoles; Resolution; Scientific imaging; Separators; Spectroscopy; Sulfates; Vapor phases; CHARGE-TRANSFER DISSOCIATION
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.9b03036

Carbohydrate isomers with identical atomic composition cannot be distinguished by mass spectrometry. By separating the ions according to their conformation in the gas phase, ion mobility (IM) coupled to mass spectrometry is an attractive approach to overcome this issue and extend the limits of mass spectrometry in structural glycosciences. Recent technological developments have significantly increased the resolving power of ion mobility separators. One such instrument features a cyclic traveling-wave IM separator integrated in a quadrupole/time-of-flight mass spectrometer. This system allows for multipass ion separations and for pre-, intra-, and post-IM fragmentation. In the present study, we utilize this system to explore a complex mixture of oligoporphyrans derived from the enzymatic digestion of the cell wall of the red alga P. umbilicalis. We are able to deduce their complete structure using IM arrival times and the m/z of specific fragments. This approach was successfully applied for sequencing of oligoporphyrans of up to 1500 Da and included the positioning of the methyl ether and sulfate groups. The structures defined in this study by IM-MS/MS agree with those found in the past but use much more time-consuming analytical approaches. This study also revealed some so far undescribed structures, present at very low abundance. In addition, the results made it possible to compare the abundance of the different isomers released by the enzyme and to draw further conclusions on the specificity of β-porphyranase and more particularly on its accommodation tolerance of anhydro-bridges in subsites. Finally, a separation of two isomers with very similar mobility was obtained after 58 passes around the cIM, with an estimated resolving power of 920 for these triply charged species, confirming the structures attributed to these two isomers.