Kitta Kazumi, Ohnishi-Kameyama Mayumi, Moriyama Tatsuya, Ogawa Tadashi, Kawamoto Shinichi
National Food Research Institute, Research Planning and Coordination Division, Tsukuba, Ibaraki 305-8642, Japan.
Anal Biochem. 2006 Apr 15;351(2):290-7. doi: 10.1016/j.ab.2005.12.030. Epub 2006 Jan 13.
Two-dimensional electrophoresis with immobilized pH gradient (IPG) followed by acetic acid/urea-polyacrylamide gel electrophoresis (AU-PAGE) was developed for the detection of low-molecular weight food allergens. Wheat proteins were used to test the applicability of AU-PAGE for the analysis of food allergens. Isoelectric focusing (IEF) for first dimension was performed with IPG pH 3-10. AU-PAGE was performed as a second-dimensional electrophoresis and high resolution was obtained, especially for proteins below 15 kDa. For immunodetection, the proteins resolved on AU gel were transferred to a polyvinylidene difluoride membrane. The assembly of semidry electroblotting for AU gel was set reversed as for sodium dodecyl sulfate (SDS)-PAGE gel. The electroblotted membrane was immunolabeled with serum from a radio-allergosorbent test-positive individual for wheat to identify allergenic proteins. Protein spots strongly recognized by the patient's serum were chosen for further analysis. Mass spectrometry analysis revealed that these proteins were alpha-amylase/trypsin inhibitors and lipid transfer protein. The system developed in this study was shown to be useful as a standard protocol for the separation of low-molecular weight proteins. Moreover, the IPG strips on which IEF was performed could be used either for SDS-PAGE or AU-PAGE by only changing equilibrating conditions, allowing for a wide range of allergen analysis.
采用固定化pH梯度(IPG)二维电泳,随后进行乙酸/尿素-聚丙烯酰胺凝胶电泳(AU-PAGE)来检测低分子量食物过敏原。使用小麦蛋白来测试AU-PAGE在食物过敏原分析中的适用性。一维等电聚焦(IEF)采用pH 3-10的IPG进行。AU-PAGE作为二维电泳进行,获得了高分辨率,尤其是对于低于15 kDa的蛋白质。为了进行免疫检测,将在AU凝胶上分离的蛋白质转移到聚偏二氟乙烯膜上。AU凝胶的半干电印迹组装设置与十二烷基硫酸钠(SDS)-PAGE凝胶相反。将电印迹膜用来自小麦放射性变应原吸附试验阳性个体的血清进行免疫标记,以鉴定过敏原蛋白。选择被患者血清强烈识别的蛋白点进行进一步分析。质谱分析表明,这些蛋白质是α-淀粉酶/胰蛋白酶抑制剂和脂质转移蛋白。本研究开发的系统被证明可作为分离低分子量蛋白质的标准方案。此外,仅通过改变平衡条件,进行IEF的IPG条带可用于SDS-PAGE或AU-PAGE,从而实现广泛的过敏原分析。