Garberi J C, Macario A J, Conway de Macario E
J Bacteriol. 1985 Oct;164(1):1-6. doi: 10.1128/jb.164.1.1-6.1985.
Hybridomas were constructed with spleen cells from mice immunized against Methanosarcina barkeri 227. The reaction with the resulting monoclonal antibodies identified two antigenic determinants. Determinant 8A is present in M. barkeri 227, where it is accessible to antibody on whole bacterial cells. 8A is undetectable in (or absent from) M. barkeri R1M3, an immunologically closely related strain. Determinant 8C is present in both strains, but with M. barkeri 227 it is found only in extracts and cannot be demonstrated in whole cells. It therefore appears to be hidden. A soluble form of antigen 8A (antigen 227) was obtained treating whole M. barkeri 227 cells with absolute methanol. This antigen was further purified by affinity chromatography with antibody 8A. Chemical and immunochemical analyses of these preparations showed that antigen 227 is a high-molecular-weight (4 X 10(5)) structure composed mainly of one carbohydrate, glucose, and small amounts of amino acids. Its solubility properties suggest that this molecule is associated with a lipid moiety.
用免疫过巴氏甲烷八叠球菌227的小鼠脾细胞构建杂交瘤。与所得单克隆抗体的反应鉴定出两个抗原决定簇。决定簇8A存在于巴氏甲烷八叠球菌227中,在整个细菌细胞上可被抗体识别。8A在免疫关系密切的菌株巴氏甲烷八叠球菌R1M3中无法检测到(或不存在)。决定簇8C在两种菌株中都存在,但在巴氏甲烷八叠球菌227中,它仅存在于提取物中,在完整细胞中无法证实。因此它似乎是隐藏的。通过用无水甲醇处理完整的巴氏甲烷八叠球菌227细胞获得了抗原8A(抗原227)的可溶形式。该抗原通过用抗体8A进行亲和层析进一步纯化。对这些制剂的化学和免疫化学分析表明,抗原227是一种高分子量(4×10⁵)结构,主要由一种碳水化合物葡萄糖和少量氨基酸组成。其溶解性表明该分子与一个脂质部分相关。