Staudacher E, Kubelka V, März L
Institut für Chemie, Universität für Bodenkultur, Vienna, Austria.
Eur J Biochem. 1992 Aug 1;207(3):987-93. doi: 10.1111/j.1432-1033.1992.tb17134.x.
The fucosyltransferase activities of three insect cell lines, MB-0503 (from Mamestra brassicae), BM-N (from Bombyx mori) and Sf-9 (from Spodoptera frugiperda), were investigated and compared with that of honeybee venom glands. Cell extracts and venom gland extracts were incubated with GDP-[14C]fucose and glycopeptides isolated from human IgG and from bovine fibrin. The labeled oligosaccharide products were released by peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase A, fluorescence marked with 2-aminopyridine and analyzed both by reversed-phase and size-fractionation HPLC. They were identified by their elution positions before and after exoglycosidase treatment in comparison with standard oligosaccharides. These experiments revealed distinct fucosylation potentials in the three cell lines tested. While MB-0503 cells, like honeybee venom glands, are able to transfer fucose into alpha 1-3 and alpha 1-6 linkage to the innermost N-acetylglucosamine, only alpha 1-6-fucosyl linkages were detected with BM-N and Sf-9 cells.
研究了三种昆虫细胞系MB - 0503(来自甘蓝夜蛾)、BM - N(来自家蚕)和Sf - 9(来自草地贪夜蛾)的岩藻糖基转移酶活性,并与蜜蜂毒腺的该活性进行了比较。将细胞提取物和毒腺提取物与GDP - [14C]岩藻糖以及从人IgG和牛纤维蛋白中分离得到的糖肽一起孵育。标记的寡糖产物用肽 - N4 -(N - 乙酰 - β - 葡糖胺基)天冬酰胺酶A释放,用2 - 氨基吡啶进行荧光标记,并通过反相高效液相色谱和尺寸排阻高效液相色谱进行分析。与标准寡糖相比,根据外切糖苷酶处理前后的洗脱位置对它们进行鉴定。这些实验揭示了所测试的三种细胞系中不同的岩藻糖基化潜力。虽然MB - 0503细胞与蜜蜂毒腺一样,能够将岩藻糖转移到α1 - 3和α1 - 6连接至最内层的N - 乙酰葡糖胺上,但在BM - N和Sf - 9细胞中仅检测到α1 - 6 - 岩藻糖基连接。