Bahraoui E, el Ayeb M, Granier C, Van Rietschoten J, Rochat H
CNRS UA 1179, Faculté de Médecine, Marseille, France.
Toxicon. 1987;25(9):957-64. doi: 10.1016/0041-0101(87)90158-9.
The antigenicity of peptide 19-28, a model of one of the major antigenic regions of toxin II of the scorpion Androctonus australis Hector was tested in different solid phase radioimmunoassay systems. The type of the solid phase and the mode of binding the synthetic peptide to the phase had a considerable effect on the resulting antigenicity. Two subpopulations of anti-toxin II antibodies were purified by affinity chromatography, one on Sepharose-peptide 19-28, the other on sepharose-toxin. The native or chemically modified toxin bound in the same way to these subpopulations. Denatured toxin was only poorly recognized by these antibodies. This suggests that the antibodies purified on peptide 19-28 recognize the same conformation dependent antigenic surface as do total anti-toxin antibodies.
对肽19 - 28(澳大利亚杀人蝎(Androctonus australis Hector)毒素II主要抗原区域之一的模型)的抗原性在不同的固相放射免疫分析系统中进行了检测。固相的类型以及合成肽与固相的结合方式对所得抗原性有相当大的影响。通过亲和层析纯化了抗毒素II抗体的两个亚群,一个在琼脂糖 - 肽19 - 28上,另一个在琼脂糖 - 毒素上。天然或化学修饰的毒素以相同方式与这些亚群结合。变性毒素只能被这些抗体微弱识别。这表明在肽19 - 28上纯化的抗体与总抗毒素抗体识别相同的构象依赖性抗原表面。