Tamura Y, Kijima M, Ohishi K, Takahashi T, Suzuki S, Nakamura M
National Veterinary Assay Laboratory, Tokyo, Japan.
J Gen Microbiol. 1992 Mar;138(3):537-42. doi: 10.1099/00221287-138-3-537.
Five monoclonal antibodies (mAbs) directed against the flagellin of Clostridium chauvoei were used to analyse the structural and antigenic characteristics on the bacterial flagellar surface. Immune electron microscopy showed that three protective mAbs recognized the surfaced-exposed epitopes on the flagellar filament of this bacteria. In contrast, two non-protective mAbs recognized internal epitopes of the flagellar filament. These findings have been confirmed by ELISA using mAbs absorbed with whole cells of C. chauvoei possessing flagella. Competitive binding assays showed that protective mAbs indicated reciprocal competition, while each of the non-protective mAbs had topographically distinct epitopes. Moreover, immunoblotting analysis with cyanogen-bromide-cleaved flagellin showed that protective mAbs may preferentially recognize conformational epitopes, whilst one of the non-protective mAbs may recognize a linear and conformation-independent epitope in the flagellin of C. chauvoei.
使用五种针对产气荚膜梭菌鞭毛蛋白的单克隆抗体(mAb)来分析细菌鞭毛表面的结构和抗原特性。免疫电子显微镜显示,三种保护性单克隆抗体识别该细菌鞭毛丝上暴露于表面的表位。相比之下,两种非保护性单克隆抗体识别鞭毛丝的内部表位。使用被具有鞭毛的产气荚膜梭菌全细胞吸收的单克隆抗体进行的ELISA已证实了这些发现。竞争性结合试验表明,保护性单克隆抗体显示出相互竞争,而每种非保护性单克隆抗体具有拓扑学上不同的表位。此外,用溴化氰裂解的鞭毛蛋白进行的免疫印迹分析表明,保护性单克隆抗体可能优先识别构象表位,而其中一种非保护性单克隆抗体可能识别产气荚膜梭菌鞭毛蛋白中的线性且不依赖构象的表位。