Analysis of chain and blood group type and branching pattern of sialylated oligosaccharides by negative ion electrospray tandem mass spectrometry

被引:34
作者
Chai, W
Piskarev, VE
Mulloy, B
Liu, Y
Evans, PG
Osborn, HMI
Lawson, AM
机构
[1] Univ London Imperial Coll Sci Technol & Med, MRC, Glycosci Lab, Fac Med, Harrow HA1 3UJ, Middx, England
[2] Russian Acad Sci, Inst Organoelement Cpds, Moscow 117813, Russia
[3] Natl Inst Biol Stand & Controls, Potters Bar EN6 3QG, Herts, England
[4] Univ Reading, Sch Chem, Reading RG6 6AD, Berks, England
[5] Univ Reading, Sch Pharm, Reading RG6 6AD, Berks, England
基金
英国医学研究理事会;
关键词
D O I
10.1021/ac051606e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We previously reported sequence determination of neutral oligosaccharides by negative ion electrospray tandem mass spectrometry on a quadrupole-orthogonal time-of-flight instrument with high sensitivity and without the need of derivatization. In the present report, we extend our strategies to sialylated oligosaccharides for analysis of chain and blood group types together with branching patterns. A main feature in the negative ion mass spectrometry approach is the unique double glycosidic cleavage induced by 3-glycosidic substitution, producing characteristic D-type fragments which can be used to distinguish the type 1 and type 2 chains, the blood group related Lewis determinants, 3,6-disubstituted core branching patterns, and to assign the structural details of each of the branches. Twenty mono- and disialylated linear and branched oligosaccharides were used for the investigation, and the sensitivity achieved is in the femtomole range. To demonstrate the efficacy of the strategy, we have determined a novel complex disialylated and monofucosylated tridecasaccharide that is based on the lacto-N-decaose core. The structure and sequence assignment was corroborated by :methylation analysis and H-1 NMR spectroscopy.
引用
收藏
页码:1581 / 1592
页数:12
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