Formation of sugar radical cations from collision-induced dissociation of non-covalent complexes with S-nitroso thiyl radical precursors

• Published in: International journal of mass spectrometry Vol. 378; pp. 95 - 106
• Main Authors: Osburn, Sandra, Williams, Spencer J., O’Hair, Richard A.J.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 15.02.2015
• Subjects: Collision-induced dissociation; Non-covalent complex; S-nitrosocysteine; Saccharides; S-nitrosocysteine; Collision-induced dissociation; Saccharides; Non-covalent complex
• ISSN: 1387-3806; 1873-2798
• DOI: 10.1016/j.ijms.2014.07.020

[Display omitted] •Sugar radical cations were generated from non-covalent complexes via the CID sequence: [H3NXSNO+M]+→[H3NXS+M]+→[M]+.•Deuterium labelling reveals that [M]+ is formed by H atom abstraction from a sugar C–H bond followed by H+ transfer.•Yields of [H3NXS+M]+ and [M]+ are influenced by M and X. Monosaccharides give high yields of [H3NXS+M]+ for X=(CH2)2.•For di- through tetrasaccharides, high yields of [H3NXS+M]+ occur when X=(CH2)3 and (CH2)4.•For maltopentose, maltohexose, and maltoheptose very little of [H3NXS+M]+ is formed, regardless of the amine thiol used. A ‘bio-inspired’ method has been developed for generating sugar radical cations by multistage mass spectrometry (MS4) experiments involving collision-induced dissociation (CID) of protonated non-covalent complexes between a sugar and an S-nitrosylated thiol amine, [H3NXSNO+M]+ (where X=(CH2)2, (CH2)3, (CH2)4, CH(CO2H)CH2 and CH(CO2CH3)CH2). In the first stage of CID (MS2), homolysis of the S–NO bond unleashes a thiyl radical to give the non-covalent radical cation, [H3NXS+M]+. It was found that complexes containing S-nitroso cysteamine (X=(CH2)2) produced the most abundant radical cations for monosaccharides, while for larger sugars, the most abundant radical cations were generated from the S-nitroso derivatives of 3-amino-1-propanethiol (X=(CH2)3) and 4-amino-1-butanethiol (X=(CH2)4). CID (MS3) of the radical cation complex resulted in the dissociation of the non-covalent complex to generate the sugar radical cation [M]+. Deuterium labelling studies reveal that this process involves abstraction of a hydrogen atom from a C–H bond of the sugar coupled with proton transfer to the sugar. The fragmentation reactions of the radical cation, [M]+, were studied by another stage of CID (MS4). In this work, the scope of the method was established, particularly for the S–NO bond homolysis (MS2) and [M]+ formation (MS3) steps. Twenty-six different sugars were examined and radical cations could be generated for polysaccharides of varying lengths, as well as for the methyl pyranosides of a range of monosaccharides.