Comparison of high- and low-energy collision-induced. Dissociation tandem mass spectrometry in the analysis of glycoalkaloids and their aglycons

被引:29
作者
Claeys, M
VandenHeuvel, H
Chen, S
Derrick, PJ
Mellon, FA
Price, KR
机构
[1] UNIV WARWICK, WARWICK INST MASS SPECTROMETRY, COVENTRY CV4 7AL, W MIDLANDS, ENGLAND
[2] INST FOOD RES, NORWICH LAB, NORWICH NR4 7UA, NORFOLK, ENGLAND
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/1044-0305(95)00636-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Four aglycons (tomatidine, demissidine, solanidine, and solasodine) and three glycoalkaloids (alpha-tomatine, alpha-chaconine, and alpha-solanine) have been analyzed by positive ion liquid sec ondary ion high-energy and low-energy collision-induced dissociation (CID) tandem mass spectrometry, performed on a four-sector (EBEB) and a hybrid (EBQQ) instrument, respectively. Both high- and low-energy collision-induced dissociation mass spectra of [M + H](+) ions of these compounds provided structural information that aided the characterization of the different aglycons and of the carbohydrate sequence and linkage sites in the glycoalkaloids. Low-energy CID favors charge-driven fragmentation of the aglycon rings, whilst high-energy CID spectra are more complex and contain additional ions that appear to result from charge-remote fragmentations, multiple cleavages, or complex charge-driven rearrangements. With respect to the structural characterization of the carbohydrate part, low-energy CID fragmentations of sugar residues in the glycoalkaloids generate Y-n(+) ions and some low intensity Z(n)(+) ions; the high-energy spectra also exhibit strong (1,5)X(n)(+) ions, formed by multiple cleavage of the sugar ring, and significant Z(n)(+) ions.
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页码:173 / 181
页数:9
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