Structural analysis of underivatized neutral human milk oligosaccharides in the negative ion mode by nano-electrospray MSn (Part 1:: Methodology)

被引:138
作者
Pfenninger, A
Karas, M
Finke, B
Stahl, B
机构
[1] Goethe Univ Frankfurt, Inst Pharmaceut Chem, Bioctr, D-60439 Frankfurt, Germany
[2] Numico Res Grp, Friedrichsdorf, Taunus, Germany
关键词
D O I
10.1016/S1044-0305(02)00645-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Underivatized neutral oligosaccharides from human milk were analyzed by nano-electrospray ionization (ESI) using a quadrupole ion trap mass spectrometer (QIT-MS) in the negative-ion mode. Under these conditions neutral oligosaccharides are observed as deprotonated molecules [M - H](-) with high intensity. CID-experiments of these species with the charge localized at the reducing end lead to C-type fragment ions forming a "new" reducing end. Fragmentations are accompanied by cross-ring cleavages that yield information about linkages of internal monosaccharides. Several isomeric compounds with distinct structural features, such as different glycosidic linkages, fucosylation and branching sites were investigated. The rules governing the fragmentation behavior of this class of oligosaccharides were elucidated and tested for a representative number of certain isomeric glycoforms using the MS/MS and MSn capabilities of the QIT. On the basis of the specific fragmentation behavior of deprotonated molecules, the position of fucoses and the linkage type (Gal beta1-->3 GlcNAc or Gal beta1-->4 GlcNAc) could be determined and linear and branched could be differentiated. Rules could be established which can be applied in further investigations of these types of oligosaccharides even from heterogenous mixtures. (C) 2002 American Society for Mass Spectrometry.
引用
收藏
页码:1331 / 1340
页数:10
相关论文
共 64 条
[1]   Tandem mass spectrometry of alkali cationized polysaccharides in a quadrupole ion trap [J].
Asam, MR ;
Glish, GL .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1997, 8 (09) :987-995
[2]   High sensitivity analysis of neutral underivatized oligosaccharides by nanoelectrospray mass spectrometry [J].
Bahr, U ;
Pfenninger, A ;
Karas, M ;
Stahl, B .
ANALYTICAL CHEMISTRY, 1997, 69 (22) :4530-4535
[3]  
BAHR U, 1998, P 46 ASMS C MASS SPE, P2
[4]  
BIER ME, 1997, ELECTROSPRAY IONIZAT, P235
[5]   Alkaline degradation of oligosaccharides coupled with matrix-assisted laser desorption/ionization Fourier transform mass spectrometry: A method for sequencing oligosaccharides [J].
Cancilla, MT ;
Penn, SG ;
Lebrilla, CB .
ANALYTICAL CHEMISTRY, 1998, 70 (04) :663-672
[6]   Negative ion electrospray mass spectrometry of neutral underivatized oligosaccharides [J].
Chai, WG ;
Piskarev, V ;
Lawson, AM .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :651-657
[7]   PREPARATION AND DESORPTION MASS-SPECTROMETRY OF PERMETHYL AND PERACETYL DERIVATIVES OF OLIGOSACCHARIDES [J].
DELL, A .
METHODS IN ENZYMOLOGY, 1990, 193 :647-660
[8]   IDENTIFICATION OF INTERGLYCOSIDIC LINKAGES AND SUGAR CONSTITUENTS IN DISACCHARIDE SUBUNITS OF LARGER GLYCOSIDES BY TANDEM MASS-SPECTROMETRY [J].
DOMON, B ;
MULLER, DR ;
RICHTER, WJ .
ORGANIC MASS SPECTROMETRY, 1989, 24 (05) :357-359
[9]   A SYSTEMATIC NOMENCLATURE FOR CARBOHYDRATE FRAGMENTATIONS IN FAB-MS MS SPECTRA OF GLYCOCONJUGATES [J].
DOMON, B ;
COSTELLO, CE .
GLYCOCONJUGATE JOURNAL, 1988, 5 (04) :397-409
[10]   Glycobiology: Toward understanding the function of sugars [J].
Dwek, RA .
CHEMICAL REVIEWS, 1996, 96 (02) :683-720