Minami R, Fujibayashi S, Igarashi C, Ishikawa Y, Wagatsuma K, Nakao T, Tsugawa S
Clin Chim Acta. 1984 Feb 28;137(2):179-87. doi: 10.1016/0009-8981(84)90178-5.
Using a high performance liquid chromatography method, degradation products of heparan sulfate (HS) and dermatan sulfate (DS) were investigated after incubation of control and alpha-L-iduronidase-deficient fibroblasts with HS or DS. Characteristic elution profiles of the degradation products were obtained from the respective alpha-L-iduronidase-deficient fibroblasts. Moreover, alpha-L-iduronidase in control fibroblasts was resolved into two distinct components, forms A and B, on DEAE-cellulose column chromatography. Form A alpha-L-iduronidase could degrade HS, but not DS. Conversely, form B alpha-L-iduronidase could not degrade HS, but could degrade DS.
采用高效液相色谱法,在对照和成纤维细胞α-L-艾杜糖醛酸酶缺陷型的成纤维细胞与硫酸乙酰肝素(HS)或硫酸皮肤素(DS)孵育后,对其降解产物进行了研究。从各自的α-L-艾杜糖醛酸酶缺陷型成纤维细胞中获得了降解产物的特征洗脱图谱。此外,对照成纤维细胞中的α-L-艾杜糖醛酸酶在DEAE-纤维素柱色谱上被分离为两种不同的组分,即A和B型。A型α-L-艾杜糖醛酸酶可降解HS,但不能降解DS。相反,B型α-L-艾杜糖醛酸酶不能降解HS,但可降解DS。