Trowbridge I S, Hyman R
Cell. 1979 Jul;17(3):503-8. doi: 10.1016/0092-8674(79)90258-7.
The glycosylation defect of Thy-1-mutant lymphomas of the class E complementation group has been identified as a block in the synthesis of the lipid-linked oligosaccharide precursor of the asparagine-linked oligosaccharides of glycoproteins. Two major lipid-linked oligosaccharides were isolated from the mutant cells. Both oligosaccharides were smaller than the lipid-linkid oligosaccharides of wild-type lymphomas and, in contrast to the lipid-linked oligosaccharides isolated from wild-type cells, both were resistant to digestion with endoglycosidase H. The oligosaccharides of newly synthesized polypeptides in class E Thy-1-cells were also resistant to endoglycosidase H digestion, providing strong evidence that they are derived from the abnormal lipid-linked oligosaccharides.
E 类互补组 Thy-1 突变淋巴瘤的糖基化缺陷已被确定为糖蛋白天冬酰胺连接寡糖的脂质连接寡糖前体合成过程中的一个阻断环节。从突变细胞中分离出了两种主要的脂质连接寡糖。这两种寡糖都比野生型淋巴瘤的脂质连接寡糖小,并且与从野生型细胞中分离出的脂质连接寡糖不同,它们对内切糖苷酶 H 的消化具有抗性。E 类 Thy-1 细胞中新合成多肽的寡糖对内切糖苷酶 H 的消化也具有抗性,这有力地证明它们源自异常的脂质连接寡糖。