John E. Coligan, Thomas J. Kindt, Richard M. Krause
{"title":"Structure of the streptococcal groups A, A-variant and C carbohydrates","authors":"John E. Coligan, Thomas J. Kindt, Richard M. Krause","doi":"10.1016/0161-5890(78)90105-0","DOIUrl":null,"url":null,"abstract":"<div><p>Structural studies on the Groups A, A-variant and C carbohydrates of β-hemolytic streptococci indicate that they have in common a polyrhamnose core. The A-variant carbohydrate consists solely of this polyrhamnose structure which has been shown to contain alternating α1, 2-and α1, 3-linked rhamnose units. In agreement with results first published by Heidelberger and his coworkers (Estrada-Parra<em>et al</em>., 1963), the Group A carbohydrate has been shown to contain<em>N</em>-acetylgulcosamine residues attached to the 3-position of the 1, 2-linked rhamnose units in this polyrhamnose structure. These<em>N</em>-acetylglucosamine residues impart group-specificity to the Group A carbohydrate. The Group C carbohydrate differs from the Group A carbohydrate by having 3-<em>O</em>-α-<em>N</em>-acetylgalactosaminosyl-<em>N</em>-acetylgalactosamine units attached to the 3-position of the polyrhamnose structure. These<em>N</em>-acetylgalactosamine disaccharides are capable of inhibiting the binding of Group C carbohydrate to anti-Group C sera and are cross-reactive with the Forssman antigen.</p></div>","PeriodicalId":13265,"journal":{"name":"Immunochemistry","volume":"15 10","pages":"Pages 755-760"},"PeriodicalIF":0.0000,"publicationDate":"1978-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0161-5890(78)90105-0","citationCount":"85","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunochemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0161589078901050","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 85
Abstract
Structural studies on the Groups A, A-variant and C carbohydrates of β-hemolytic streptococci indicate that they have in common a polyrhamnose core. The A-variant carbohydrate consists solely of this polyrhamnose structure which has been shown to contain alternating α1, 2-and α1, 3-linked rhamnose units. In agreement with results first published by Heidelberger and his coworkers (Estrada-Parraet al., 1963), the Group A carbohydrate has been shown to containN-acetylgulcosamine residues attached to the 3-position of the 1, 2-linked rhamnose units in this polyrhamnose structure. TheseN-acetylglucosamine residues impart group-specificity to the Group A carbohydrate. The Group C carbohydrate differs from the Group A carbohydrate by having 3-O-α-N-acetylgalactosaminosyl-N-acetylgalactosamine units attached to the 3-position of the polyrhamnose structure. TheseN-acetylgalactosamine disaccharides are capable of inhibiting the binding of Group C carbohydrate to anti-Group C sera and are cross-reactive with the Forssman antigen.
对β-溶血性链球菌A、A-变体和C群碳水化合物的结构研究表明,它们具有共同的多鼠糖核。a型碳水化合物仅由这种鼠李糖结构组成,该结构已被证明含有交替的α 1,2和α 1,3连接鼠李糖单元。与Heidelberger和他的同事(Estrada-Parraet al., 1963)首次发表的结果一致,A族碳水化合物已被证明含有n -乙酰氨基葡萄糖残基,附着在这种鼠李糖结构中1,2连接鼠李糖单元的3位上。这些乙酰氨基葡萄糖残基赋予A族碳水化合物基团特异性。C族碳水化合物与A族碳水化合物的不同之处在于,聚鼠糖结构的3位上有3-O-α- n -乙酰半乳糖胺基- n -乙酰半乳糖胺单元。这些乙酰半乳糖胺二糖能够抑制C组碳水化合物与抗C组血清的结合,并与Forssman抗原发生交叉反应。