Suresh M R, Cuello A C, Milstein C
Proc Natl Acad Sci U S A. 1986 Oct;83(20):7989-93. doi: 10.1073/pnas.83.20.7989.
A chemical selection procedure has been used to prepare a hybrid hybridoma cell line (P4C1) following fusion of two previously established hybridomas secreting antiperoxidase and antisubstance P, respectively. P4C1 secretes bispecific monoclonal antibody alongside the two parental antibodies, with no visible inactive heterologous heavy-light chain pairs. The bispecific monoclonal antibody is thus easy to purify in excellent yields. The advantage of its monovalency for one antigen and simultaneous binding of a marker enzyme has been explored for its potential use in competitive immunoassays. Its use in immunocytochemistry led to major improvements in sensitivity, signal-to-noise ratio, simplification of staining procedures, and ultrastructural preservation of subcellular elements. Particularly remarkable was that, unlike conventional procedures, the immunoreaction with the bispecific monoclonal antibody was homogeneously distributed across the entire thickness of a 50-micron section.
采用化学选择程序,在分别分泌抗过氧化物酶和抗P物质的两种先前建立的杂交瘤融合后,制备了一种杂交杂交瘤细胞系(P4C1)。P4C1除分泌两种亲本抗体外,还分泌双特异性单克隆抗体,且无可见的无活性异源重链-轻链对。因此,该双特异性单克隆抗体易于纯化,产率极高。已探索了其对一种抗原的单价性以及同时结合标记酶的优势,以了解其在竞争性免疫测定中的潜在用途。其在免疫细胞化学中的应用使灵敏度、信噪比、染色程序简化以及亚细胞成分的超微结构保存方面有了重大改进。特别值得注意的是,与传统程序不同,与双特异性单克隆抗体的免疫反应在50微米切片的整个厚度上均匀分布。