Characterization of protein and mannan polysaccharide antigens of yeasts, moulds, and actinomycetes.

E Reiss, M Huppert, R Cherniak
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引用次数: 37

Abstract

Antigens in coccidioidin were compared with purified subfractions via tandem immunoelectrophoresis (IEP) and by a combination of advancing line and crossed IEP. Rocket IEP was suitable for titrating the reactions and showing the relationship between column fractions. These techniques required multicomponent antisera produced by hyperimmunization over many months and by the use of known standard migration pairs. The IEP variations were used to chart the development of antisera against coccidioidin factors, to monitor antigen purifications, and to test the immunochemical homogeneity of an isolated antigen. Mannose-based heteroglycans of Cryptococcus neoformans were recovered from the culture filtrate. After precipitation of the major viscous glucuronoxylomannan (GXM) with ethanol or cetyltrimethylammonium bromide, the supernate is reserved because it contains a galactoxylomannan (GalXM). After removal of glucuronic acid from the GXM, the resulting xylomannan of serotype A was amenable to 13C-nuclear magnetic resonance (NMR) spectrometry; it revealed nonreducing xylose, alpha-1,3-mannose, and alpha-1,2/1,3 disubstituted mannose, thus confirming by an independent means what was previously known. The characterization sequence of GalXM included: (1) gas-liquid chromatography (GLC) of neutral sugars as peracetylated aldononitriles; (2) methylation-fragmentation GLC mass spectrometry to determine the glycosidic linkages; and (3) 13C-NMR showing similarities to mannan of Saccharomyces cerevisiae. Affinity chromatography of the GalXM on concanavalin A separated the galactoxylo component from an adsorbed mannoprotein. Selection of monoclonal antibodies (MAbs) relies on presumptive enzyme immunoassays (EIAs) or radioimmunoassays for rapid screening of clones and for determination of isotypes; however, higher resolution confirmatory tests are needed to obtain MAbs of desired specificity. MAbs against Candida tropicalis mannan were labeled with horseradish peroxidase to use for detecting mannan in serum. MAbs against the partially purified "m" factor of histoplasmin were characterized by the enzyme-linked immunoelectro-transfer blot technique (EITB), revealing unsuspected complexity in the antigen. Secreted proteins of Nocardia asteroides were isoelectrically focused; three proteins, identified by EITB as promising to be specific for that actinomycete, were cut out of gels and used to immunize mice for production of MAbs. The fimbriae of Actinomyces viscosus and A. naeslundii that mediate lactose-reversible coagglutination with Streptococcus sanguis have been used to evoke MAbs.(ABSTRACT TRUNCATED AT 400 WORDS)

酵母、霉菌和放线菌蛋白质和甘露聚糖抗原的表征。
采用串联免疫电泳(IEP)和推进系与杂交免疫电泳相结合的方法,对球虫蛋白抗原与纯化亚组分进行了比较。火箭IEP法适用于滴定反应,并能显示柱分数之间的关系。这些技术需要通过数月的过度免疫和使用已知的标准迁移对产生多组分抗血清。IEP变化被用来绘制抗球虫因子血清的发展图,监测抗原纯化,并测试分离抗原的免疫化学均匀性。从培养滤液中回收了新型隐球菌的甘露糖基杂聚糖。在用乙醇或十六烷基三甲基溴化铵沉淀主要粘性葡萄糖醛酸甘露聚糖(GXM)后,上清液被保留,因为它含有半乙酰甘露聚糖(GalXM)。从GXM中去除葡萄糖醛酸后,得到血清型A的木甘露聚糖符合13c核磁共振(NMR)谱法;它揭示了不还原性木糖,α -1,3-甘露糖和α -1,2/1,3双取代甘露糖,从而以独立的方式证实了之前已知的东西。GalXM的表征序列包括:(1)中性糖作为过乙酰化醛腈的气液色谱(GLC);(2)甲基化-碎片GLC质谱法测定糖苷键;(3) 13C-NMR显示与酿酒酵母甘露聚糖相似。半胱甘肽A上的半胱甘肽亲和层析将半胱甘肽成分与吸附的甘露蛋白分离。单克隆抗体(mab)的选择依赖于假定的酶免疫测定(EIAs)或放射免疫测定,用于快速筛选克隆和确定同种型;然而,需要更高分辨率的确证试验来获得所需特异性的单克隆抗体。用辣根过氧化物酶标记抗热带假丝酵母甘露聚糖单抗,用于血清甘露聚糖检测。针对部分纯化的组织浆蛋白“m”因子的单克隆抗体通过酶联免疫电转移印迹技术(EITB)进行了鉴定,揭示了抗原的复杂性。小行星诺卡菌分泌蛋白等电聚焦;三种蛋白被EITB鉴定为有希望对该放线菌具有特异性,从凝胶中切割出来,用于免疫小鼠以产生单克隆抗体。粘胶放线菌和A. naeslundii的菌毛介导乳糖可逆凝血链球菌已被用于产生单克隆抗体。(摘要删节为400字)
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