Shuttleworth C A, Berry L, Wilson N H
Arch Oral Biol. 1982;27(8):645-50. doi: 10.1016/0003-9969(82)90187-x.
Confluent dental pulp fibroblast cultures incorporated L-[3H]-fucose in a linear manner with time into non-diffusible macromolecules over 24 h. Ascorbate supplementation did not appear to alter the amount or type of macromolecules. Equilibrium CsCl-density-gradient centrifugation established that the [3H]-fucose-labelled macromolecules released into the medium were predominantly glycoproteins. Sodium dodecyl sulphate-polyacrylamide-gel electrophoresis showed that the major fucosylated glycoprotein had an apparent molecular weight of 230,000, but several other species were also seen. The major fucosylated glycoprotein was fibronectin by its affinity for gelatin and its immunoprecipitation with a specific anti-(cold-insoluble globulin).
融合的牙髓成纤维细胞培养物在24小时内随时间以线性方式将L-[3H]-岩藻糖掺入不可扩散的大分子中。补充抗坏血酸似乎并未改变大分子的数量或类型。平衡氯化铯密度梯度离心表明,释放到培养基中的[3H]-岩藻糖标记的大分子主要是糖蛋白。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示,主要的岩藻糖基化糖蛋白的表观分子量为230,000,但也可见其他几种糖蛋白。通过其对明胶的亲和力及其与特异性抗(冷不溶性球蛋白)的免疫沉淀,主要的岩藻糖基化糖蛋白是纤连蛋白。