Nilsson R, Sjögren H O
J Immunol Methods. 1984 Jan 20;66(1):17-25. doi: 10.1016/0022-1759(84)90243-6.
A high non-specific binding of immunoglobulins to plastic surfaces was noted with a number of rat sera, when tested in an indirect 125I-labeled protein-A assay for detection of cell-surface-bound rat immunoglobulins of various classes and IgG subclasses. This type of non-specific binding was found with all types of Ig. The degree of binding varied with the type of test plate used and fluctuated with time among sera drawn sequentially from the same donors. Coating test wells with fetal calf serum supplemented with BSA, gelatin or fibrinogen did not eliminate the reactions. The immunoglobulins bind directly to the polystyrene, and not to antigens present in fetal calf serum or autoantigens in rat serum. Two different approaches were used to eliminate the nonspecific reaction. When living cells were used as target antigens, exclusively cell-bound radioactivity was eluted with the non-ionic detergent Nonidet P40, which solubilizes the cell membrane without breaking the protein-A/rabbit IgG, rabbit IgG/rat Ig, or rat Ig/plastic interactions. When rat serum antibodies are tested on target antigens adsorbed on non-tissue culture grade plates, non-specific binding may be avoided by including 0.05% Tween 20 in the incubation mixture.
在用于检测各类及IgG亚类细胞表面结合型大鼠免疫球蛋白的间接¹²⁵I标记蛋白A试验中,发现许多大鼠血清中的免疫球蛋白与塑料表面存在高度非特异性结合。所有类型的Ig均存在这种非特异性结合。结合程度随所用试验板类型而异,且在从同一供体依次采集的血清中随时间波动。用补充了牛血清白蛋白、明胶或纤维蛋白原的胎牛血清包被试验孔并不能消除反应。免疫球蛋白直接与聚苯乙烯结合,而非与胎牛血清中的抗原或大鼠血清中的自身抗原结合。采用了两种不同方法来消除非特异性反应。当使用活细胞作为靶抗原时,仅用非离子去污剂Nonidet P40洗脱细胞结合的放射性,该去污剂可溶解细胞膜而不破坏蛋白A/兔IgG、兔IgG/大鼠Ig或大鼠Ig/塑料的相互作用。当在非组织培养级平板上吸附的靶抗原上检测大鼠血清抗体时,可通过在孵育混合物中加入0.05%吐温20来避免非特异性结合。