Ogata S, Misumi Y, Miki K, Ikehara Y
Eur J Biochem. 1986 Dec 1;161(2):315-20. doi: 10.1111/j.1432-1033.1986.tb10449.x.
We analyzed the asparagine-linked oligosaccharide chains of rat haptoglobin which were synthesized and secreted by hepatocytes in primary culture. When the cells were incubated with either [3H]mannose, [3H]galactose, or [3H]fucose, all the radioactive precursors were incorporated into the beta subunit of haptoglobin. [3H]Mannose-labeled haptoglobin was purified from the culture medium by immunoaffinity chromatography, and [3H]oligosaccharides were prepared by strong alkali-borohydride treatment. The oligosaccharides obtained were analyzed by anion-exchange high-performance liquid chromatography, concanavalin-A--Sepharose chromatography and Bio-Gel P-4 chromatography before and after sequential exoglycosidase digestions. The oligosaccharides labeled with [3H]fucose or [3H]galactose were also characterized by the above methods. The results indicate that rat haptoglobin contains two complex-type oligosaccharide chains in each beta subunit; one with a possible structure of ( +/- NeuAc----Gal beta----GlcNAc beta----)3(Man alpha----)2 Man beta----GlcNAc----( +/- Fuc alpha----)GlcNAc and the other with ( +/- NeuAc----Gal beta----GlcNAc beta----Man alpha----)2 Man beta----GlcNAc----( +/- Fuc alpha----)GlcNAc.
我们分析了原代培养的肝细胞合成并分泌的大鼠触珠蛋白的天冬酰胺连接的寡糖链。当细胞与[³H]甘露糖、[³H]半乳糖或[³H]岩藻糖一起孵育时,所有放射性前体都掺入到触珠蛋白的β亚基中。通过免疫亲和色谱从培养基中纯化[³H]甘露糖标记的触珠蛋白,并通过强碱硼氢化物处理制备[³H]寡糖。在进行外切糖苷酶顺序消化之前和之后,通过阴离子交换高效液相色谱、伴刀豆球蛋白A-琼脂糖凝胶色谱和Bio-Gel P-4色谱对获得的寡糖进行分析。还用上述方法对用[³H]岩藻糖或[³H]半乳糖标记的寡糖进行了表征。结果表明,大鼠触珠蛋白的每个β亚基含有两条复合型寡糖链;一条可能的结构为(+/-NeuAc----Galβ----GlcNAcβ----)3(Manα----)2Manβ----GlcNAc----(+/-Fucα----)GlcNAc,另一条为(+/-NeuAc----Galβ----GlcNAcβ----Manα----)2Manβ----GlcNAc----(+/-Fucα----)GlcNAc。