Roth J
Department of Pathology, University of Zürich, Switzerland.
Histochem Cell Biol. 1996 Jul;106(1):79-92. doi: 10.1007/BF02473203.
High resolution immunolabeling applying the protein A-gold technique and carbohydrate cytochemistry using lectin-gold labeling on Lowicryl K4M and thawed-frozen thin sections are most useful approaches for the detection of protein antigens and lectin binding sites in intracellular organelles and the plasma membrane. They provided the basis for modern electron microscopic studies on protein glycosylation reactions and the identification of their subcellular localization as reviewed here. These studies have demonstrated organelle subcompartments and the cell type-specific compartmentation of endoplasmic reticulum and Golgi apparatus-associated glycosylation reactions. The other subject reviewed in this paper is cell surface glycoconjugates, as they are expressed in relation to specific cell types present in various organs and during cellular differentiation processes.
在Lowicryl K4M和解冻冷冻薄切片上应用蛋白A-金技术进行高分辨率免疫标记以及使用凝集素-金标记进行碳水化合物细胞化学,是检测细胞内细胞器和质膜中蛋白质抗原及凝集素结合位点的最有用方法。它们为现代电子显微镜研究蛋白质糖基化反应及其亚细胞定位的鉴定提供了基础,本文对此进行了综述。这些研究已经证明了细胞器亚区室以及内质网和高尔基体相关糖基化反应的细胞类型特异性区室化。本文综述的另一个主题是细胞表面糖缀合物,因为它们在各种器官中存在的特定细胞类型以及细胞分化过程中表达。