Structural information on oligosaccharides was obtained by post-source decay matrix-assisted laser desorp tion/ionization mass spectrometry. A systematic study of derivatized oligosaccharides showed that products relatively aminated with benzylamine allow the formation of [ M + HI + molecular specie
Structure analysis of trivalent glycoclusters by post-source decay matrix-assisted laser desorption/ionization mass spectrometry
✍ Scribed by Havlíček, Vladimír; Kieburg, Christoffer; Novák, Petr; Bezouška, Karel; Lindhorst, Thisbe K.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 270 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
✦ Synopsis
Post-source decay (PSD) matrix-assisted laser desorption/ionization time-of-Ñight mass spectra were found to be useful for the structural elucidation of a series of tris [ 2-(glycosylthiourylene)ethyl ] amines. The reported fragmentation behaviours of [ M + H ] ', [ M + Na ] ' and [ M Ô H ]ions di †er from each other signiÐcantly ; however, they can be compared to tree pruning in every case. Whereas detailed structural information on unprotected glycoclusters is obtained from all PSD experiments, only the positive-ion mode can be used to gain relevant information about the acetylated glycoclusters.
📜 SIMILAR VOLUMES
Sulfonated azo molecules containing hydroxy groups ortho-or para-to the azo linkage exhibit azo/ hydrazone tautomerism, which affects their coloristic properties and also the fragmentation pathways observed in tandem mass spectrometry. Electrospray tandem MS and matrix-assisted laser desorption/ ion
Partial 18 O-labeling of peptides has been applied to post-source decay experiments in a matrix-assisted laser desorption/ionization time-of-flight mass spectrometer. The ions which originate from the carboxyl terminus of a peptide partially retain 18 O atoms which have readily been incorporated int
A series of synthetic cyclic decapeptides and other smaller cyclic peptides were analyzed using matrixassisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. The investigated compounds were cyclized in a head-to-tail manner and contained non-proteinaceous amino acids, such