Savelkoul H F, Greeve A A, Rijkers G T, Marwitz P A, Benner R
Department of Cell Biology, Immunology and Genetics, Erasmus University, Rotterdam, The Netherlands.
J Immunol Methods. 1988 Jun 28;111(1):31-7. doi: 10.1016/0022-1759(88)90056-7.
A rapid and efficient procedure is described for the coupling of proteins (protein A, ovalbumin, albumin and chicken gamma globulin) to sheep red blood cells (SRBC) to be used in antigen-specific or protein A plaque assays. This modification of the original procedure has three distinct features: prewash of the red cells with a low concentration of essentially freshly prepared CrCl3, use of a relatively high concentration of CrCl3 in the reaction mixture and a coupling time of only 4 min. Protein A plaque assays performed with such target cells have the same sensitivity as those employing red cells coupled with protein A according to the original procedure. Studies with hybridomas secreting antibody specific for a protein antigen showed that antigen-specific plaque assays employing target red cells coupled with the protein antigen according to the modified procedure have the same sensitivity as the protein A plaque assay. The modified procedure greatly facilitates cellular studies on antibody formation after immunization with protein antigens.
本文描述了一种快速有效的方法,用于将蛋白质(蛋白A、卵清蛋白、白蛋白和鸡γ球蛋白)与绵羊红细胞(SRBC)偶联,以用于抗原特异性或蛋白A空斑试验。对原始方法的这种改进有三个显著特点:用低浓度的基本新鲜制备的CrCl3对红细胞进行预洗涤,在反应混合物中使用相对较高浓度的CrCl3,以及仅4分钟的偶联时间。用这种靶细胞进行的蛋白A空斑试验与按照原始方法用与蛋白A偶联的红细胞进行的试验具有相同的灵敏度。对分泌针对蛋白质抗原的特异性抗体的杂交瘤的研究表明,按照改进方法用与蛋白质抗原偶联的靶红细胞进行的抗原特异性空斑试验与蛋白A空斑试验具有相同的灵敏度。该改进方法极大地促进了在用蛋白质抗原免疫后抗体形成的细胞研究。