Shone C, Wilton-Smith P, Appleton N, Hambleton P, Modi N, Gatley S, Melling J
Appl Environ Microbiol. 1985 Jul;50(1):63-7. doi: 10.1128/aem.50.1.63-67.1985.
A monoclonal antibody (BA11) has been produced against Clostridium botulinum type A neurotoxin by the fusion of myeloma cells (P3 NS1/1-Ag4-1) with spleen cells from BALB/c mice immunized with botulinum type A neurotoxoid. The antibody bound specifically to botulinum type A neurotoxin, showing no cross-reactivity with types B and E botulinum toxins or with any of several other bacterial toxins tested. The monoclonal antibody did not bind to botulinum type A neurotoxin which had been denatured with sodium dodecyl sulfate and bound only weakly to each of the separated heavy and light subunits of the neurotoxin, suggesting a conformational requirement for the antigenic determinant of the antibody. A sensitive immunoassay for C. botulinum type A toxin with monoclonal antibody BA11 in conjunction with an enzyme amplication system has been developed which allows detection of 5 to 10 mouse 50% lethal doses ml-1 of purified neurotoxin. The assay was equally sensitive when applied to the detection of crude toxin in food stuffs; the average value for the minimum level of detectable toxin in extracts of tinned salmon or corned beef was 9 +/- 3.1 mouse 50% lethal doses ml-1.
通过骨髓瘤细胞(P3 NS1/1-Ag4-1)与用A型肉毒类毒素免疫的BALB/c小鼠的脾细胞融合,制备了一种抗A型肉毒杆菌神经毒素的单克隆抗体(BA11)。该抗体与A型肉毒杆菌神经毒素特异性结合,与B型和E型肉毒杆菌毒素或所测试的其他几种细菌毒素均无交叉反应。该单克隆抗体不与经十二烷基硫酸钠变性的A型肉毒杆菌神经毒素结合,且仅与神经毒素分离的重链和轻链亚基中的每一个微弱结合,这表明抗体的抗原决定簇需要特定构象。已开发出一种使用单克隆抗体BA11结合酶放大系统的A型肉毒杆菌毒素灵敏免疫测定法,该方法可检测出每毫升5至10个小鼠50%致死剂量的纯化神经毒素。当应用于检测食品中的粗毒素时,该测定法同样灵敏;罐装鲑鱼或腌牛肉提取物中可检测到的毒素最低水平的平均值为每毫升9±3.1个小鼠50%致死剂量。