Identification of a novel inner-core oligosaccharide structure in Neisseria meningitidis lipopolysaccharide

被引:12
作者
Cox, AD
Wright, JC
Gidney, MAJ
Lacelle, S
Plested, JS
Martin, A
Moxon, ER
Richards, JC
机构
[1] Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
[2] Univ Oxford, Inst Mol Med, John Radcliffe Hosp, Oxford OX1 2JD, England
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2003年 / 270卷 / 08期
关键词
lipopolysaccharide; mass spectrometry; Neisseria meningitidis; NMR; oligosaccharide;
D O I
10.1046/j.1432-1033.2003.03535.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structure of the lipopolysaccharide (LPS) from three Neisseria meningitidis strains was elucidated. These strains were nonreactive with mAbs that recognize common inner-core epitopes from meningococcal LPS. It is well established that the inner core of meningococcal LPS consists of a diheptosyl-N -acetylglucosamine unit, in which the distal heptose unit (Hep II) can carry P Etn at the 3 or 6 position or not at all, and the proximal heptose residue (Hep I) is substituted at the 4 position by a glucose residue. Additional substitution at the 3 position of Hep II with a glucose residue is also a common structural feature in some strains. The structures of the O-deacylated LPSs and core oligosaccharides of the three chosen strains were deduced by a combination of monosaccharide analysis, NMR spectroscopy and MS. These analyses revealed the presence of a structure not previously identified in meningococcal LPS, in which an additional beta-configured glucose residue was found to substitute Hep I at the 2 position. This provided the structural basis for the nonreactivity of LPS with these mAbs. The determination of this novel structural feature identified a further degree of variability within the inner-core oligosaccharide of meningococcal LPS which may contribute to the interaction of meningococcal strains with their host.
引用
收藏
页码:1759 / 1766
页数:8
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