Arnaud P, Wilson G B, Koistinen J, Fudenberg H H
J Immunol Methods. 1977;16(3):221-31. doi: 10.1016/0022-1759(77)90200-9.
An improved method is described for direct localization of human serum proteins in polyacrylamide gel with simultaneous determination of their isoelectric points (pI). The technique employs isoelectric focusing in thin-layer polyacrylamide gels to separate the serum proteins and the pH gradient is read at 4 degrees C with a dual-membrane surface microelectrode. Subsequently, the desired proteins are localized by immunofixation in the gel or by immunofixation-printing onto cellulose acetate strips soaked in specific antiserum. No sectioning of the electrofocused gel is necessary, and the entire technique can be completed in less than 14 h. When this method is applied to the detection of the genetic variants of alpha-1-antitrypsin (alpha-1-protease inhibitor) (A1Pi system), the results indicate that it can be used to specifically localize serum proteins whose pI's differ by as little as 0.01 pH units. The resolution afforded is especially evident in the analysis of A1Pi M variants.
本文描述了一种改进的方法,用于在聚丙烯酰胺凝胶中直接定位人血清蛋白,并同时测定其等电点(pI)。该技术采用薄层聚丙烯酰胺凝胶中的等电聚焦来分离血清蛋白,并在4℃下用双膜表面微电极读取pH梯度。随后,通过凝胶中的免疫固定或通过免疫固定印迹到浸泡在特异性抗血清中的醋酸纤维素条上来定位所需的蛋白质。无需对等电聚焦凝胶进行切片,整个技术可在不到14小时内完成。当该方法应用于检测α-1-抗胰蛋白酶(α-1-蛋白酶抑制剂)(A1Pi系统)的遗传变异体时,结果表明它可用于特异性定位pI相差仅0.01个pH单位的血清蛋白。在A1Pi M变异体的分析中,所提供的分辨率尤为明显。