Atassi M Z, Sakata S
Biochim Biophys Acta. 1980 Aug 21;624(2):573-8. doi: 10.1016/0005-2795(80)90097-5.
Recently, we reported the synthesis and immunochemistry of two peptides designed, by complementarity and surface-simulation synthesis, to mimic antibody-combining sites against two antigenic sites of lysozyme. In the present work antibodies were raised against one of these peptides, which is complementary to antigenic site 3 of lysozyme, to determine whether these antibodies will react with anti-lysozyme antibodies. Radioiodinated antipeptide antibodies were bound by immunoadsorbents of the immune IgG from two goats anti-lysozyme antisera but not by adsorbents of myoglobin, non-immune goat IgG or immune IgG of antisera against cytochrome c. The binding of anti-peptide antibodies to adsorbents of anti-lysozyme antibodies was fully inhibited by free lysozyme but not by bovine serum albumin, human hemoglobin A, horse cytochrome c or bovine ribonuclease A. Thus, antisera against an antibody-combining site can be raised by immunizing with a peptide which probably does not exist in the antibody but is designed by surface-simulation synthesis to mimic an antibody-combining site.
最近,我们报道了通过互补性和表面模拟合成设计的两种肽的合成及免疫化学性质,这两种肽旨在模拟针对溶菌酶两个抗原位点的抗体结合位点。在本研究中,针对其中一种与溶菌酶抗原位点3互补的肽制备了抗体,以确定这些抗体是否会与抗溶菌酶抗体发生反应。放射性碘化抗肽抗体能被来自两只山羊抗溶菌酶抗血清的免疫IgG免疫吸附剂结合,但不能被肌红蛋白、非免疫山羊IgG或抗细胞色素c抗血清的免疫IgG吸附剂结合。游离溶菌酶可完全抑制抗肽抗体与抗溶菌酶抗体吸附剂的结合,而牛血清白蛋白、人血红蛋白A、马细胞色素c或牛核糖核酸酶A则不能。因此,可以通过用一种可能不存在于抗体中但通过表面模拟合成设计以模拟抗体结合位点的肽进行免疫来制备针对抗体结合位点的抗血清。