Hopwood J J
Carbohydr Res. 1979 Mar;69:203-16. doi: 10.1016/s0008-6215(00)85765-1.
Radioactive disaccharide substrates for alpha-L-iduronidase, beta-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase have been prepared from heparin by deaminative cleavage followed by reduction with NaBT4. Six disaccharides were isolated from this reaction mixture and identified. Acid hydrolysis of the major disaccharide, O-(alpha-L-idopyranosyluronic acid 2-sulfate)-(1 linked to 4)-(2,5-anhydro-D-mannitol-l-t 6-sulfate (IdAs--Ms), produced 48% of O-(alpha-L-idopyranosyluronic acid)-(1 linked to 4)-(2,5-anhydro-D-mannitol-l-t 6-sulfate) (IdA--Ms) and 25% of O-(alpha-L-idopyranosyluronic acid)-(1 linked to 4)-2,5-anhydro-D-mannitol-l-t. The most-sensitive substrate for determining alpha-L-iduronidase activity was IdA--Ms which, when incubated with leucocyte and skin-fibroblast homogenates prepared from patients having a deficiency of alpha-L-iduronidase (Mucopolysaccharidosis Type I; MPS-I), was hydrolysed to yield 2,5-anhydro-D-mannitol-l-t 6-sulfate at a rate 50-times less than that found for normal control-preparations. Similarly, O-(beta-D-glucopyranosyluronic acid)-(1 linked to 4)-(2,5-anhydro-D-mannitol-l-t 6-sulfate) was degraded by whole-cell homogenates prepared from beta-D-glucuronidase-deficient (Mucopolysaccharidosis, Type VII) fibroblasts, to yield 2,5-anhydro-D-mannitol-l-t 5-sulfate at a rate 60-times less that that found for MPS-I and normal control-preparations. IdAs--Ms was degraded by 2-sulfo-L-iduronate 2-sulfatase at a rate more than 45-times greater than that found for O-(alpha-L-idopyranosyluronic acid 2-sulfate)-(1 linked to 4)-2,5-anhydro-D-mannitol-l-t. C-6 Sulfation of the anhydro-D-mannitol-l-t residue is an important structural determinant in the mechanism of action of both alpha-L-iduronidase and 2-sulfo-L-iduronate 2-sulfatase on disaccharide substrates.
已通过脱氨基裂解,随后用NaBT4还原,从肝素制备了用于α-L-艾杜糖醛酸酶、β-D-葡萄糖醛酸酶和2-磺酸-L-艾杜糖醛酸2-硫酸酯酶的放射性二糖底物。从该反应混合物中分离并鉴定出六种二糖。主要二糖O-(α-L-吡喃艾杜糖醛酸2-硫酸酯)-(1→4)-(2,5-脱水-D-甘露糖醇-1,6-二硫酸酯)(IdAs--Ms)的酸水解产生48%的O-(α-L-吡喃艾杜糖醛酸)-(1→4)-(2,5-脱水-D-甘露糖醇-1,6-二硫酸酯)(IdA--Ms)和25%的O-(α-L-吡喃艾杜糖醛酸)-(1→4)-2,5-脱水-D-甘露糖醇-1。用于测定α-L-艾杜糖醛酸酶活性的最敏感底物是IdA--Ms,当它与从缺乏α-L-艾杜糖醛酸酶(I型粘多糖贮积症;MPS-I)的患者制备的白细胞和皮肤成纤维细胞匀浆一起孵育时,其水解产生2,5-脱水-D-甘露糖醇-1,6-二硫酸酯的速率比正常对照制剂低50倍。同样,O-(β-D-吡喃葡萄糖醛酸)-(1→4)-(2,5-脱水-D-甘露糖醇-1,6-二硫酸酯)被从缺乏β-D-葡萄糖醛酸酶(VII型粘多糖贮积症)的成纤维细胞制备的全细胞匀浆降解,产生2,5-脱水-D-甘露糖醇-1,5-二硫酸酯的速率比MPS-I和正常对照制剂低60倍。IdAs--Ms被2-磺酸-L-艾杜糖醛酸2-硫酸酯酶降解的速率比O-(α-L-吡喃艾杜糖醛酸2-硫酸酯)-(1→4)-2,5-脱水-D-甘露糖醇-1高45倍以上。脱水-D-甘露糖醇-1,6-二硫酸酯残基的C-6硫酸化是α-L-艾杜糖醛酸酶和2-磺酸-L-艾杜糖醛酸2-硫酸酯酶对二糖底物作用机制中的重要结构决定因素。