Turco S J, Robbins P W
J Biol Chem. 1979 Jun 10;254(11):4560-7.
Following the rapid enzymatic transfer of an oligosaccharide (GlcNAc2Man9Glc3) from a lipid carrier to endogenous protein acceptors in membrane preparations from NIL fibroblasts, the transferred oligosaccharide chain undergoes processing. Protein-bound oligosaccharides, released from the polypeptide backbone by treatment with endo-beta-N-acetylglucosaminidase H, were analyzed by gel filtration and by susceptibility to alpha-mannosidase digestion. The initial stages of this processing in vitro consist of sequential excision of 3 glucose residues prior to the removal of mannose residues. The array of oligosaccharides generated in vitro by membrane preparations from NIL cells appears to be identical with processed oligosaccharides derived in vivo in intact NIL cells.
在来自NIL成纤维细胞的膜制剂中,寡糖(GlcNAc2Man9Glc3)从脂质载体快速酶促转移至内源性蛋白质受体后,转移的寡糖链会进行加工处理。通过用内切β-N-乙酰葡糖胺糖苷酶H处理从多肽主链释放的与蛋白质结合的寡糖,通过凝胶过滤和对α-甘露糖苷酶消化的敏感性进行分析。体外这种加工处理的初始阶段包括在去除甘露糖残基之前依次切除3个葡萄糖残基。NIL细胞的膜制剂在体外产生的寡糖阵列似乎与完整NIL细胞体内衍生的加工后寡糖相同。