Direct detection of idiotypic determinants on blotted monoclonal antibodies.

Annales d'immunologie Pub Date : 1982-07-01
C Petit, M E Sauron, M Gilbert, J Thèze
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Abstract

The protein-blotting technique has been tested as a mean to study the expression of idiotypic determinants. A monoclonal BALB/c antipoly (Glu60-Ala30-Tyr10) GAT antibody (G5) was caused to migrate on SDS gel and transferred to a nitrocellulose filter. To facilitate the renaturation of the idiotypic determinants, the blotted proteins were incubated in NP40 buffer, immediately after the transfer. The ability of two anti-idiotypic sera to detect two defined idiotypic specificities of the blotted G5 molecules was investigated. When G5 was electrophoresed on SDS gel under non-reducing conditions, a specific detection of two idiotypic specificities of the G5-blotted molecules was obtained. On the other hand, when G5 was migrated under reducing conditions, none of the two antiidiotypic sera gave a staining of the heavy and the light chains. This result indicates that molecules expressing conformational idiotypic determinants can be detected by protein-blotting technique after migration on SDS gel. Moreover, this suggests the possible interest of this technique to analyse non-antibody molecules bearing idiotypic determinants.

印迹单克隆抗体独特型决定因子的直接检测。
蛋白质印迹技术已被测试作为研究独特型决定因子表达的手段。单克隆BALB/c抗聚(Glu60-Ala30-Tyr10) GAT抗体(G5)在SDS凝胶上迁移,并转移到硝化纤维素过滤器上。为了促进独特型决定因子的再生,印迹蛋白在转移后立即在NP40缓冲液中孵育。研究了两种抗独特型血清检测印迹G5分子的两种明确的独特型特异性的能力。当G5在非还原条件下在SDS凝胶上电泳时,获得了G5印迹分子的两种独特型特异性的特异性检测。另一方面,当G5在还原条件下迁移时,两种抗独特型血清均未出现重链和轻链的染色。这表明表达构象独特型决定因子的分子在SDS凝胶上迁移后可以通过蛋白印迹技术检测到。此外,这表明该技术可能对分析具有独特型决定因子的非抗体分子感兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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