Capillary electrophoresis to measure sulfoesterase activity on chondroitin sulfate and heparin derived disaccharides.

A Pervin, K Gu, R J Linhardt
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Abstract

Capillary electrophoresis was used to assay sulfoesterase activity on sulfated disaccharides derived from chondroitin sulfate, dermatan sulfate and heparin. The three sulfoesterases studied were chondro-4-O-sulfatase (EC 3.1.6.9) and chondro-6-O-sulfatase (EC 3.1.6.10) from Proteus vulgaris and heparo-2-O-sulfatase from Flavobacterium heparinum. Capillary electrophoresis was used to analyse sulfated disaccharide before and after sulfoesterase treatment and a change in migration time was indicative of the presence of sulfoesterase activity. This assay was used both on purified sulfoesterases and on minor sulfoesterase contaminants present in other enzyme preparations. The high sensitivity of capillary electrophoresis permits the elimination of 35S-radiolabeled substrates normally required to assay sulfoesterases. The high resolution of capillary electrophoresis allows the use of this assay on impure enzyme preparations containing high protein concentrations.

毛细管电泳测定硫酸软骨素和肝素衍生双糖的硫酯酶活性。
采用毛细管电泳法测定硫酸软骨素、硫酸皮聚糖和肝素提取的硫酸二糖的硫酯酶活性。所研究的3种磺化酯酶分别是普通变形杆菌(Proteus vulgaris)的4- o-硫酸酯酶(EC 3.1.6.9)和6- o-硫酸酯酶(EC 3.1.6.10)以及肝黄杆菌(Flavobacterium heparinum)的2- o-硫酸酯酶。用毛细管电泳法对磺胺酯酶处理前后的硫酸化双糖进行了分析,发现迁移时间的变化表明存在磺胺酯酶活性。该试验既用于纯化的磺胺酯酶,也用于其他酶制剂中存在的少量磺胺酯酶污染物。毛细管电泳的高灵敏度允许消除通常需要测定硫酯酶的35s放射性标记底物。毛细管电泳的高分辨率允许在含有高浓度蛋白质的不纯酶制剂上使用该测定。
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