Angström J, Teneberg S, Milh M A, Larsson T, Leonardsson I, Olsson B M, Halvarsson M O, Danielsson D, Näslund I, Ljungh A, Wadström T, Karlsson K A
Department of Medical Biochemistry, Göteborg University, Medicinaregatan 9A, S-413 90 Göteborg, Sweden.
Glycobiology. 1998 Apr;8(4):297-309. doi: 10.1093/glycob/8.4.297.
The possible role of glycosphingolipids as adhesion receptors for the human gastric pathogen Helicobacter pylori was examined by use of radiolabeled bacteria, or protein extracts from the bacterial cell surface, in the thin-layer chromatogram binding assay. Of several binding specificities found, the binding to lactosylceramide is described in detail here, the others being reported elsewhere. By autoradiography a preferential binding to lactosylceramide having sphingosine/phytosphingosine and 2-D hydroxy fatty acids was detected, whereas lactosylceramide having sphingosine and nonhydroxy fatty acids was consistently nonbinding. A selective binding of H. pylori to lactosylceramide with phytosphingosine and 2-D hydroxy fatty acid was obtained when the different lactosylceramide species were incorporated into liposomes, but only in the presence of cholesterol, suggesting that this selectivity may be present also in vivo . Importantly, lactosylceramide with sphingosine and hydroxy fatty acids does not bind in this assay. Furthermore, a lactosylceramide-based binding pattern obtained for different trisaccharide glycosphingolipids is consistent with the assumption that this selectivity is due to binding of a conformation of lactosylceramide in which the oxygen of the 2-D fatty acid hydroxyl group forms a hydrogen bond with the Glc hydroxy methyl group, yielding an epitope presentation different from other possible conformers. An alternative conformation that may come into consideration corresponds to the crystal structure found for cerebroside, in which the fatty acid hydroxyl group is free to interact directly with the adhesin. By isolating glycosphingolipids from epithelial cells of human stomach from seven individuals, a binding of H.pylori to the diglycosylceramide region of the non-acid fraction could be demonstrated in one of these cases. Mass spectrometry showed that the binding-active sample contained diglycosylceramides with phytosphingosine and 2-D hydroxy fatty acids with 16-24 carbon atoms in agreement with the results related above.
利用放射性标记细菌或细菌细胞表面蛋白提取物,通过薄层层析结合试验研究了糖鞘脂作为人类胃部病原体幽门螺杆菌粘附受体的可能作用。在发现的几种结合特异性中,本文详细描述了与乳糖神经酰胺的结合情况,其他结合特异性在其他地方报道。通过放射自显影检测到,幽门螺杆菌优先结合具有鞘氨醇/植物鞘氨醇和2-D羟基脂肪酸的乳糖神经酰胺,而具有鞘氨醇和非羟基脂肪酸的乳糖神经酰胺始终不结合。当将不同种类的乳糖神经酰胺掺入脂质体中时,幽门螺杆菌会选择性地结合含有植物鞘氨醇和2-D羟基脂肪酸的乳糖神经酰胺,但仅在有胆固醇存在的情况下,这表明这种选择性在体内也可能存在。重要的是,在该试验中,含有鞘氨醇和羟基脂肪酸的乳糖神经酰胺不结合。此外,不同三糖糖鞘脂获得的基于乳糖神经酰胺的结合模式与以下假设一致,即这种选择性是由于乳糖神经酰胺构象的结合,其中2-D脂肪酸羟基的氧与葡萄糖羟基甲基形成氢键,产生与其他可能构象体不同的表位呈现。可能考虑的另一种构象对应于脑苷脂的晶体结构,其中脂肪酸羟基可自由直接与粘附素相互作用。通过从7名个体的人胃上皮细胞中分离糖鞘脂,在其中1例中可证明幽门螺杆菌与非酸性部分的二糖神经酰胺区域结合。质谱分析表明,具有结合活性的样品含有含有植物鞘氨醇和具有16-24个碳原子的2-D羟基脂肪酸的二糖神经酰胺,这与上述结果一致。