{"title":"兔溶血微球菌肽聚糖和葡萄糖- n -乙酰氨基诺曼醛酸聚合物特异性抗体的分离与鉴定。","authors":"M Wikler","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The antibody response of rabbits to Micrococcus lysodeikticus is characterized by the production of a high concentration of antibodies which manifest markedly reduced heterogenicity. The specificity of these antibodies was studied and it revealed that M. lysodeikticus contains 2 major antigens: both the glucose-N-acetyl-aminomannuronic acid polymer obtained by formamide extraction of the cell walls and peptidoglycan solubilized by ultrasonic treatment gave precipitin reactions with hyperimmune antisera. By means of inhibition studies of the glucose-mannose polymer specificity, glucose appeared as the immunodominant sugar in the majority of antibodies studied. Inhibitions studies also confirmed that both the glycan and peptide moieties constitute antigenic determinants of M. lysodeikticus peptidoglycan. Antibodies to the glucose-mannose-polymer and the peptidoglycan were specifically fractionated by use of immunoadsorbents formed from lysozyme solubilized cell walls and activated Sepharose. Both antibody specificities showed a limited heterogeneity by isoelectric focusing. Finally, because antisera to M. lysodeikticus are a rich source of antibodies to peptidoglycan, emphasis is placed on the possible usefulness of this system for studies of clonal dominance.</p>","PeriodicalId":23768,"journal":{"name":"Zeitschrift fur Immunitatsforschung, experimentelle und klinische Immunologie","volume":"149 2-4","pages":"193-200"},"PeriodicalIF":0.0000,"publicationDate":"1975-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolation and characterization of homogenous rabbit antibodies to Micrococcus lysodeikticus with specificity to the peptidoglycan and to the glucose-N-acetylaminomannuronic acid polymer.\",\"authors\":\"M Wikler\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The antibody response of rabbits to Micrococcus lysodeikticus is characterized by the production of a high concentration of antibodies which manifest markedly reduced heterogenicity. The specificity of these antibodies was studied and it revealed that M. lysodeikticus contains 2 major antigens: both the glucose-N-acetyl-aminomannuronic acid polymer obtained by formamide extraction of the cell walls and peptidoglycan solubilized by ultrasonic treatment gave precipitin reactions with hyperimmune antisera. By means of inhibition studies of the glucose-mannose polymer specificity, glucose appeared as the immunodominant sugar in the majority of antibodies studied. Inhibitions studies also confirmed that both the glycan and peptide moieties constitute antigenic determinants of M. lysodeikticus peptidoglycan. Antibodies to the glucose-mannose-polymer and the peptidoglycan were specifically fractionated by use of immunoadsorbents formed from lysozyme solubilized cell walls and activated Sepharose. Both antibody specificities showed a limited heterogeneity by isoelectric focusing. Finally, because antisera to M. lysodeikticus are a rich source of antibodies to peptidoglycan, emphasis is placed on the possible usefulness of this system for studies of clonal dominance.</p>\",\"PeriodicalId\":23768,\"journal\":{\"name\":\"Zeitschrift fur Immunitatsforschung, experimentelle und klinische Immunologie\",\"volume\":\"149 2-4\",\"pages\":\"193-200\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift fur Immunitatsforschung, experimentelle und klinische Immunologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift fur Immunitatsforschung, experimentelle und klinische Immunologie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
兔对溶血微球菌的抗体反应的特点是产生高浓度的抗体,其异质性明显降低。对这些抗体的特异性进行了研究,发现溶血分枝杆菌含有2种主要抗原:甲酰胺提取细胞壁得到的葡萄糖- n -乙酰氨基氨醛酸聚合物和超声处理溶解的肽聚糖与高免疫抗血清发生沉淀反应。通过对葡萄糖-甘露糖聚合物特异性的抑制研究,葡萄糖在大多数抗体中显示为免疫优势糖。抑制研究也证实,多糖和肽段都是溶歧杆菌肽聚糖的抗原决定因素。利用溶菌酶溶解的细胞壁和活化的葡聚糖形成的免疫吸附剂,对葡萄糖-甘露糖-聚合物和肽聚糖的抗体进行特异性分离。通过等电聚焦,两种抗体特异性均表现出有限的异质性。最后,由于溶血分枝杆菌的抗血清是肽聚糖抗体的丰富来源,因此重点放在该系统在克隆优势研究中的可能用途上。
Isolation and characterization of homogenous rabbit antibodies to Micrococcus lysodeikticus with specificity to the peptidoglycan and to the glucose-N-acetylaminomannuronic acid polymer.
The antibody response of rabbits to Micrococcus lysodeikticus is characterized by the production of a high concentration of antibodies which manifest markedly reduced heterogenicity. The specificity of these antibodies was studied and it revealed that M. lysodeikticus contains 2 major antigens: both the glucose-N-acetyl-aminomannuronic acid polymer obtained by formamide extraction of the cell walls and peptidoglycan solubilized by ultrasonic treatment gave precipitin reactions with hyperimmune antisera. By means of inhibition studies of the glucose-mannose polymer specificity, glucose appeared as the immunodominant sugar in the majority of antibodies studied. Inhibitions studies also confirmed that both the glycan and peptide moieties constitute antigenic determinants of M. lysodeikticus peptidoglycan. Antibodies to the glucose-mannose-polymer and the peptidoglycan were specifically fractionated by use of immunoadsorbents formed from lysozyme solubilized cell walls and activated Sepharose. Both antibody specificities showed a limited heterogeneity by isoelectric focusing. Finally, because antisera to M. lysodeikticus are a rich source of antibodies to peptidoglycan, emphasis is placed on the possible usefulness of this system for studies of clonal dominance.