Nardelli B, McHugh L, Mage M
Division of Cancer Biology and Diagnosis, National Cancer Institute, Bethesda, MD 20892.
J Immunol Methods. 1989 Jun 21;120(2):233-9. doi: 10.1016/0022-1759(89)90247-0.
We have developed a soluble macromolecular conjugation reagent, polyacrylamide-streptavidin (PASA), for the simplified preparation of multivalent protein-protein conjugates. Soluble linear polyacrylamide, with a molecular weight of approximately 10(6), has carboxyl groups generated by limited alkaline hydrolysis. It is then activated with carbodiimide, separated from excess carbodiimide, and conjugated to streptavidin. The resulting conjugate, which has approximately 20 streptavidin residues per molecule, can bind biotinylated proteins to produce homo- or heteroconjugates of known composition. We have used this technique to prepare soluble multivalent heteroligating antibody conjugates that can bind either of two antigenically distinct cell lines, as well as reagents that specifically label murine tumor cells with different MHC class I antigens. The method is potentially useful for making multivalent arrays of epitopes for measuring low affinity interactions such as that between the T cell receptor and MHC molecules, as well as for making immunotoxins, tumor labelling conjugates, and complex immunogens.
我们开发了一种可溶性大分子偶联试剂,即聚丙烯酰胺-链霉亲和素(PASA),用于简化多价蛋白质-蛋白质偶联物的制备。分子量约为10⁶的可溶性线性聚丙烯酰胺通过有限的碱水解产生羧基。然后用碳二亚胺将其活化,与过量的碳二亚胺分离,并与链霉亲和素偶联。所得的偶联物每个分子约有20个链霉亲和素残基,可结合生物素化的蛋白质以产生已知组成的同型或异型偶联物。我们已使用该技术制备了可结合两种抗原性不同细胞系中任一种的可溶性多价异源连接抗体偶联物,以及用不同的MHC I类抗原特异性标记鼠肿瘤细胞的试剂。该方法对于制备用于测量低亲和力相互作用(如T细胞受体与MHC分子之间的相互作用)的多价表位阵列,以及制备免疫毒素、肿瘤标记偶联物和复合免疫原可能是有用的。