Bahr G M, Carelli C, Audibert F, Modabber F, Chedid L
Mol Immunol. 1982 May;19(5):737-45. doi: 10.1016/0161-5890(82)90375-3.
Antibodies to N-acetyl-muramyl-L-alanyl-D-isoglutamine (MDP) were produced in rabbits by injection of MDP conjugated to various carriers [bovine gamma globulin (BGG), methylated BSA or sheep erythrocytes]. The anti-MDP was assayed by a direct enzyme-linked immunosorbent assay (ELISA) using horse radish peroxidase linked to MDP-Lys. Various derivatives of MDP were employed in an inhibition of ELISA for analysis of specificity of antibodies and study of the relationship of configuration to biological activity. The results confirmed previous findings that MDP alone is not immunogenic but can act as a hapten when conjugated to carriers. The antibodies were shown to be primarily directed against the muramyl residue. Modifications of this region of MDP yielded derivatives with weak reactivity against anti-MDP, while some changes of other regions had no effect on its antigenicity. Optical isomers of MDP had reduced activity as compared to MDP and polymeric MDP was a strong inhibitor. The structure and function relationship is discussed for some derivatives.
通过向兔子注射与各种载体(牛γ球蛋白(BGG)、甲基化牛血清白蛋白或绵羊红细胞)偶联的N-乙酰胞壁酰-L-丙氨酰-D-异谷氨酰胺(MDP),制备了抗MDP抗体。使用与MDP-Lys连接的辣根过氧化物酶,通过直接酶联免疫吸附测定(ELISA)对抗MDP进行检测。使用MDP的各种衍生物进行ELISA抑制试验,以分析抗体的特异性,并研究构象与生物活性的关系。结果证实了先前的发现,即单独的MDP不具有免疫原性,但与载体偶联时可作为半抗原。结果表明,这些抗体主要针对胞壁酰残基。MDP这一区域的修饰产生了对抗MDP反应性较弱的衍生物,而其他区域的一些变化对其抗原性没有影响。与MDP相比,MDP的光学异构体活性降低,聚合MDP是一种强抑制剂。对一些衍生物的结构与功能关系进行了讨论。