Entrapment of normal and mutant glucose 6-phosphate dehydrogenase (G6PD) within G6PD deficient erythrocytes.

A De Flora, A Morelli, U Benatti
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引用次数: 1

Abstract

G6PD-deficient erythrocytes (Mediterranean type of this enzyme disorder) were loaded with a) normal G6PD purified to homogeneity from human erythrocytes, b) G6PD Mediterranean purified from deficient granulocytes. The first set of experiments led to complete normalization of biochemical properties of erythrocytes, as assessed by evaluating their metabolic competence under steady state conditions and under oxidative stress as well. The second type of experiment allowed us to conclude that mutant G6PD is not appreciably destroyed within the affected erythrocytes.

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正常和突变的葡萄糖6-磷酸脱氢酶(G6PD)在G6PD缺陷红细胞中的包埋。
G6PD缺陷红细胞(这种酶紊乱的地中海型)装载a)从人红细胞中纯化到均匀的正常G6PD, b)从缺陷粒细胞中纯化的G6PD地中海型。第一组实验通过评估红细胞在稳态条件下和氧化应激下的代谢能力,使红细胞的生化特性完全正常化。第二种类型的实验使我们得出结论,突变的G6PD在受影响的红细胞内没有明显的破坏。
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