Craig S, Goodchild D J
Eur J Cell Biol. 1982 Oct;28(2):251-6.
The sensitivity of detection of proteins by immunolabelling embedded and sectioned material depends upon retention of antigenicity during tissue processing. Losses in pea seed storage protein antigenicity have been assessed using a solid phase radioimmunoassay. Storage proteins adsorbed to wells of microtiter plates were treated with the various "tissue preparation" steps and reacted with 125I-antibodies to the storage proteins. The glutaraldehyde or formaldehyde fixation steps caused approximately 60% and 30% loss in antigenicity, respectively. With each subsequent preparative step, losses accumulate and following treatment with Spurr's epoxy resin reached approximately 85% and 90%, respectively. However, if Lowicryl K4M, a methacrylate-acrylate embedding medium was used, losses were retained at approximately 70% and 60%, respectively. These observations have been verified on sections of embedded material using two labelling procedures, with protein A-gold and ferritin as the markers.
通过对包埋和切片材料进行免疫标记来检测蛋白质的灵敏度取决于组织处理过程中抗原性的保留情况。已使用固相放射免疫测定法评估了豌豆种子贮藏蛋白抗原性的损失。吸附到微量滴定板孔中的贮藏蛋白经过各种“组织制备”步骤处理后,与针对贮藏蛋白的125I标记抗体发生反应。戊二醛或甲醛固定步骤分别导致约60%和30%的抗原性损失。随着后续每个制备步骤的进行,损失不断累积,在用Spurr环氧树脂处理后分别达到约85%和90%。然而,如果使用甲基丙烯酸酯 - 丙烯酸酯包埋介质Lowicryl K4M,损失分别保持在约70%和60%。这些观察结果已通过两种标记程序在包埋材料的切片上得到验证,使用蛋白A - 金和铁蛋白作为标记物。