Structural characterization of glycoporphyrins by electrospray tandem mass spectrometry |
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Authors: | Domingues M R M Domingues P Reis A Ferrer-Correia A J Tomé J P C Tomé A C Neves M G P M S Cavaleiro J A S |
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Institution: | Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal. mrd@dq.ua.pt |
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Abstract: | Porphyrin derivatives having a galactose or a bis(isopropylidene)galactose structural unit, linked by ester or ether bonds, were characterized by electrospray tandem mass spectrometry (ES-MS/MS). The electrospray mass spectra of these glycoporphyrins show the corresponding M + H](+) ions. For the glycoporphyrins with pyridyl substituents and those having a tetrafluorophenyl spacer, the doubly charged ions M + 2H](2+) were also observed in ES-MS with high relative abundance. The fragmentation of both M + H](+) and M + 2H](2+) ions exhibited common fragmentation pathways for porphyrins with the same sugar residue, independently of the porphyrin structural unit and type of linkage. ES-MS/MS of the M + H](+) ions of the galactose-substituted porphyrins gave the fragment ions M + H - C(2)H(4)O(2)](+), M + H - C(3)H(6)O(3)](+), M + H - C(4)H(8)O(4)](+) and M + H - galactose residue](+). The fragmentation of the M + 2H](2+) ions of the porphyrins with galactose shows the common doubly charged fragment ions porphyrin + H](2+), M + 2H - C(2)H(4)O(2)](2+), M + 2H - C(4)H(8)O(4)](2+), M + 2H - galactose residue](2+) and the singly charged fragment ions M + H - C(3)H(6)O(3)](+) and M + H - galactose residue](+). The fragmentation of the M + H](+) ions of glycoporphyrins with a protected galactosyl residue leads mainly to the ions M + H - CO(CH(3))(2)](+), M + H - 2CO(CH(3))(2)](+), M + H - 2CO(CH(3))(2) - CO](+), M + H - C(10)H(16)O(4)](+) and M + H - protected galactose](+). The doubly charged ions M + 2H](2+) fragment to give the doubly charged ions porphyrin + H](2+) and the singly charged ions M + H - protected galactose residue](+) and M + H - CO(CH(3))(2)](+). For the porphyrins where the sugar structural unit is linked by an ester bond, M + 2H](2+), ES-MS/MS showed a major and typical fragmentation corresponding to combined loss of a sugar structural unit and further loss of water, leading to the ion M + 2H - sugar residue - H(2)O](2+), independently of the structure of the sugar structural unit. These results show that ES-MS/MS can be a powerful tool for the characterization of the sugar structural unit of glycoporphyrins, without the need for chemical hydrolysis. |
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Keywords: | glycoporphyrins electrospray mass spectrometry tandem mass spectrometry |
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