Conformation of the hexasaccharide repeating subunit from the Vibrio cholerae O139 capsular polysaccharide

被引:22
作者
Adeyeye, J
Azurmendi, HF
Stroop, CJM
Sozhamannan, S
Williams, AL
Adetumbi, AM
Johnson, JA
Bush, CA [1 ]
机构
[1] Univ Maryland Baltimore Cty, Dept Chem & Biochem, Baltimore, MD 21250 USA
[2] Univ Maryland, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[3] Univ Maryland, Sch Med, Dept Epidemiol & Prevent Med, Baltimore, MD 21205 USA
[4] Vet Affairs Maryland Hlth Care Syst, Baltimore, MD 21202 USA
[5] Howard Univ, Dept Biol, Washington, DC 20059 USA
[6] Johns Hopkins Univ, Sch Med, Baltimore, MD 21205 USA
关键词
D O I
10.1021/bi026700t
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
In the past decade, several outbreaks of cholera have been reported to be caused by Vibrio cholerae 0 139, a strain which differs from the more common 0 1 strain in that the former is encapsulated. The hexasaccharide repeating subunit has been isolated from the V. cholerae 0139 capsular polysaccharide by digestion with a recently discovered polysaccharide lyase derived from a bacteriophage specific for this serogroup. It specifically cleaves at a single position of the 4-linked galacturonic acid producing an unsaturated sugar product in quantities for conformational studies by H-1 and C-13 NMR spectroscopy. We report conformational studies on this oligosaccharide by molecular modeling and NMR spectroscopy including nuclear Overhauser effects and residual dipolar coupling of a sample weakly oriented in liquid crystalline solution. The structure contains a tetrasaccharide epitope homologous to the human Lewis(b) blood group antigen, which adopts a relatively well-defined single conformation. Comparison of these results with those of a previously published study of the intact capsular polysaccharide indicates that the conformations of the epitope in the two cases are identical or at least closely similar. Thus, this epitope, which may be essential for the pathogenicity of this V. cholerae strain, is not a "conformational epitope" requiring a certain critical size for antigenicity as has been reported for several other bacterial capsular antigens.
引用
收藏
页码:3979 / 3988
页数:10
相关论文
共 44 条
[1]  
Albert MJ, 1996, INDIAN J MED RES, V104, P14
[2]   Phage specific for Vibrio cholerae O139 Bengal [J].
Albert, MJ ;
Bhuiyan, NA ;
Rahman, A ;
Ghosh, AN ;
Hultenby, K ;
Weintraub, A ;
Nahar, S ;
Kibriya, AKMG ;
Ansaruzzaman, M ;
Shimada, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (07) :1843-1845
[3]   Physical interpretation of residual dipolar couplings in neutral aligned media [J].
Almond, A ;
Axelsen, JB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (34) :9986-9987
[4]   Comparison of aqueous molecular dynamics with NMR relaxation and residual dipolar couplings favors internal motion in a mannose oligosaccharide [J].
Almond, A ;
Bunkenborg, J ;
Franch, T ;
Gotfredsen, CH ;
Duus, JO .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (20) :4792-4802
[5]  
Almond A, 2001, J BIOMOL NMR, V20, P351
[6]   Conformational studies of Lewis X and Lewis A trisaccharides using NMR residual dipolar couplings [J].
Azurmendi, HF ;
Martin-Pastor, M ;
Bush, CA .
BIOPOLYMERS, 2002, 63 (02) :89-98
[7]   Tracking alignment from the moment of inertia tensor (TRAMITE) of biomolecules in neutral dilute liquid crystal solutions [J].
Azurmendi, HF ;
Bush, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (11) :2426-2427
[8]   Conformational studies of blood group A and blood group B oligosaccharides using NMR residual dipolar couplings [J].
Azurmendi, HF ;
Bush, CA .
CARBOHYDRATE RESEARCH, 2002, 337 (10) :905-915
[9]   SCOPE AND LIMITATIONS OF ROTATING-FRAME NUCLEAR OVERHAUSER ENHANCEMENT SPECTROSCOPY APPLIED TO OLIGOSACCHARIDES [J].
BREG, J ;
ROMIJN, D ;
VLIEGENTHART, JFG ;
STRECKER, G ;
MONTREUIL, J .
CARBOHYDRATE RESEARCH, 1988, 183 (01) :19-34
[10]   NMR and molecular dynamics studies of the conformational epitope of the type III group B Streptococcus capsular polysaccharide and derivatives [J].
Brisson, JR ;
Uhrinova, S ;
Woods, RJ ;
vanderZwan, M ;
Jarrell, HC ;
Paoletti, LC ;
Kasper, DL ;
Jennings, HJ .
BIOCHEMISTRY, 1997, 36 (11) :3278-3292