Gärtner S, Conzelmann E, Sandhoff K
J Biol Chem. 1983 Oct 25;258(20):12378-85.
An activator protein which stimulates the degradation of globotriaosylceramide by human hepatic alpha-galactosidase (alpha-D-galactoside galactohydrolase, EC 3.2.1.22) was isolated from human liver and purified some 1300-fold. The purified activator was heat stable up to 95 degrees C, its molecular weight was estimated at 20,000 by gel filtration. Ampholyte displacement chromatography resolved the activating factor into two fractions with isoelectric points at pH 4.6 and pH 4.8, respectively, with otherwise identical properties. The protein did not stimulate the hydrolysis of the water-soluble 4-methylumbelliferyl-alpha-galactoside.
从人肝脏中分离出一种激活蛋白,它可刺激人肝脏α-半乳糖苷酶(α-D-半乳糖苷半乳糖水解酶,EC 3.2.1.22)对球三糖神经酰胺的降解,并将其纯化了约1300倍。纯化后的激活蛋白在高达95℃时仍具有热稳定性,通过凝胶过滤法估计其分子量为20,000。两性电解质置换色谱法将激活因子分离成两个组分,其等电点分别为pH 4.6和pH 4.8,其他性质相同。该蛋白不刺激水溶性4-甲基伞形酮基-α-半乳糖苷的水解。