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首页> 外文期刊>Biochemistry >Structure of the variable and conserved lipopolysaccharide oligosaccharide epitopes expressed by Haemophilus influenzae serotype b strain Eagan.
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Structure of the variable and conserved lipopolysaccharide oligosaccharide epitopes expressed by Haemophilus influenzae serotype b strain Eagan.

机译:b型流感嗜血杆菌血清Eagan株表达的可变且保守的脂多糖寡糖表位的结构。

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Lipopolysaccharide (LPS) is a major virulence determinant of Haemophilus influenzae. The organism is capable of expressing a heterogeneous population of LPS which exhibits extensive antigenic diversity among multiple oligosaccharide (OS) epitopes. Structural elucidation of variable and conserved OS epitopes of H. influenzae serotype b strain Eagan was determined by the application of high-field NMR techniques and MS-based methods on oligosaccharides obtained from LPS samples by a deacylation strategy. LPS extracted by the hot aqueous phenol method gave complex electrophoretic patterns consisting of at least six low-molecular mass bands. Electrospray ionization-mass spectrometry of O-deacylated LPS revealed a series of related structures differing in the number of hexose residues as well as subpopulations of glycoforms containing additional phosphoethanolamine (PEA) groups. It was demonstrated that the LPS contains a conserved PEA-substituted, heptose-containing trisaccharide inner core moiety attached via a KDO 4-phosphate unit to a lipid A component. Tandem MS experiments unambiguously established the presence of a KDO 4-pyrophosphoethanolamine unit in the subpopulation of LPS containing additional PEA groups. The occurrence of LPS containing this structural feature was found to be dependant on the isolation procedure used. Each heptose of the common inner core element L-alpha-D-Hepp(1-->2)-L-alpha-D-Hepp(1-->3)-L-alpha-D-Hep p(1-->5)-alpha-KDO is substituted by a hexose residue with further chain elongation from the central unit. The structures of the major glycoforms containing four (three Glcs and one Gal), five (three Glcs and two Gals), and six (three Glcs and three Gals) hexoses were determined in detail. The Hex6 glycoform contains the terminal structure, alpha-D-Galp(1-->4)-beta-D-Galp(1-->4)-beta-D-Glc, providing, for the first time, definitive structural evidence for the expression of the Pk-blood group antigen in H. influenzae LPS. Moreover, an analogue of the Hex4 glycoform was identified in which the third heptose residue carries phosphate at 0-4.
机译:脂多糖(LPS)是流感嗜血杆菌的主要毒力决定因素。该生物体能够表达LPS的异质群体,其在多个寡糖(OS)表位之间表现出广泛的抗原多样性。 b。流感嗜血杆菌血清型b株Eagan可变和保守的OS表位的结构解析通过应用高场NMR技术和基于MS的方法通过脱酰化策略从LPS样品获得的寡糖来确定。通过热苯酚水法提取的LPS给出了复杂的电泳图谱,该图谱至少由六个低分子质量带组成。 O-去酰基化LPS的电喷雾电离质谱分析显示了一系列相关结构,这些结构在己糖残基数量以及含有额外的磷酸乙醇胺(PEA)基团的糖型亚群方面有所不同。已证明,LPS包含一个保守的PEA取代的,含庚糖的三糖内核部分,该部分通过KDO 4-磷酸酯单元连接到脂质A组分上。串联MS实验明确地确定了在含有额外PEA基团的LPS亚群中存在KDO 4-焦磷酸乙醇胺单元。发现含有该结构特征的LPS的出现取决于所使用的分离程序。共同内核元素的每个庚糖L-alpha-D-Hepp(1-> 2)-L-alpha-D-Hepp(1-> 3)-L-alpha-D-Hep p(1-- > 5)-α-KDO被己糖残基取代,其中心单元的链进一步延长。详细确定了包含四个(三个Glcs和一个Gal),五个(三个Glcs和两个Gals)和六个(三个Glcs和三个Gals)己糖的主要糖型的结构。 Hex6糖型包含末端结构,即alpha-D-Galp(1-> 4)-beta-D-Galp(1-> 4)-beta-D-Glc,首次提供了确定的结构证据在流感嗜血杆菌LPS中表达Pk-血液基团抗原。此外,鉴定出Hex4糖型的类似物,其中第三个庚糖残基在0-4携带磷酸。

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