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血浆α-半乳糖苷酶A:特性及其与组织α-半乳糖苷酶的比较

Plasma alpha-galactosidase A:properties and comparisons with tissue alpha-galactosidases.

作者信息

Bishop D F, Sweeley C C

出版信息

Biochim Biophys Acta. 1978 Aug 7;525(2):399-409. doi: 10.1016/0005-2744(78)90235-8.

Abstract

The human plasma form of alpha-galactosidase A (alpha-D-galactoside galactohydrolase, EC 3.2.1.22) was highly purified and exhibited apparent Km values of 1.9 mM with 4-methylumbelliferyl-alpha-D-galactopyranoside and 0.23 mM with globotriglycosylceramide. Its inhibition with myo-inositol (Ki = 0.29 M) was similar to that observed with alpha-galactosidase A from various tissues. The plasma form of this lysosomal enzyme has a lower molecular weight of 96 600, a lower pI of 3.7 and faster electrophoretic mobility in polyacrylamide gels than the enzyme obtained from human liver. These data and the increased pI obtained after neuraminidase treatment suggest that the plasma form is an isoenzyme with a more highly sialylated carbohydrate moiety than the tissue isoenzymes.

摘要

人血浆形式的α-半乳糖苷酶A(α-D-半乳糖苷半乳糖水解酶,EC 3.2.1.22)经过高度纯化,以4-甲基伞形酮基-α-D-吡喃半乳糖苷为底物时,其表观Km值为1.9 mM,以球三糖基神经酰胺为底物时,表观Km值为0.23 mM。其被肌醇抑制(Ki = 0.29 M)的情况与从各种组织中获得的α-半乳糖苷酶A所观察到的相似。这种溶酶体酶的血浆形式分子量较低,为96600,pI较低,为3.7,在聚丙烯酰胺凝胶中的电泳迁移率比从人肝脏中获得的酶更快。这些数据以及神经氨酸酶处理后获得的升高的pI表明,血浆形式是一种同工酶,其碳水化合物部分的唾液酸化程度比组织同工酶更高。

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