Peng Z K, Simons F E, Becker A B
Department of Pediatrics, University of Manitoba, Winnipeg, Canada.
J Immunol Methods. 1991 Dec 15;145(1-2):255-8. doi: 10.1016/0022-1759(91)90335-d.
We studied the binding of dog immunoglobulins G, A, M and E to protein A and protein G. Passive cutaneous anaphylaxis (PCA) testing was used for the measurement of dog IgE and enzyme-linked immunosorbent assays (ELISA) were used for the measurements of dog IgG, IgA and IgM. Protein A from lyophilized cells of Staphylococcus aureus bound 97% of IgE, 98% of IgG, 81% of IgA, and 97% of IgM. Protein A-Sepharose CL-4B bound 87% of IgE, 100% of IgG and IgA, and 98% of IgM. In a stepwise elution with varying pH, a small amount of IgE was eluted at pH 5 and pH 6 and all the remaining Igs were eluted at pH 3 from the protein A column. In contrast to protein A, dog IgE was not bound to Protein G-Sepharose, while 100% of IgG, 95% of IgA, and 44% of IgM were bound to Protein G-Sepharose.
我们研究了犬免疫球蛋白G、A、M和E与蛋白A和蛋白G的结合情况。采用被动皮肤过敏反应(PCA)试验来检测犬IgE,并用酶联免疫吸附测定(ELISA)来检测犬IgG、IgA和IgM。来自金黄色葡萄球菌冻干细胞的蛋白A可结合97%的IgE、98%的IgG、81%的IgA和97%的IgM。蛋白A-琼脂糖凝胶CL-4B可结合87%的IgE、100%的IgG和IgA以及98%的IgM。在不同pH值的分步洗脱过程中,少量IgE在pH 5和pH 6时被洗脱,其余所有免疫球蛋白在pH 3时从蛋白A柱上被洗脱。与蛋白A不同,犬IgE不与蛋白G-琼脂糖凝胶结合,而100%的IgG、95%的IgA和44%的IgM与蛋白G-琼脂糖凝胶结合。