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用ATP的碳二亚胺衍生物使Ca2(+)、Na+K(+)和H+K(+) -ATP酶失活。

Inactivation of Ca2(+)-, Na+K(+)-, and H+K(+)-ATPases with a carbodiimide derivative of ATP.

作者信息

Murphy A J

机构信息

Department of Biochemistry, University of the Pacific, San Francisco, CA 94115.

出版信息

FEBS Lett. 1990 Apr 9;263(1):175-7. doi: 10.1016/0014-5793(90)80733-y.

Abstract

The gamma-P adduct of ATP with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (ATP-EDC) was synthesized and incubated with the Ca-ATPase of sarcoplasmic reticulum with the result that time-dependent complete loss of the enzyme's activity occurred. The inactivation required calcium and magnesium while ATP had a protective effect. ATP-EDC incubation with the NaK-ATPase and HK-ATPase produced partial (greater than 50%) inactivation, but had no effect on myosin S1, pyruvate kinase and hexokinase, suggesting that this ATP analog is a specific inactivator of the so-called 'P-type' ATPases.

摘要

合成了ATP与1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(ATP-EDC)的γ-P加合物,并将其与肌浆网的钙ATP酶一起孵温温温育,结果该酶的活性随时间完全丧失。失活需要钙和镁,而ATP具有保护作用。ATP-EDC与钠钾ATP酶和己糖激酶ATP酶温育会导致部分(大于50%)失活,但对肌球蛋白S1、丙酮酸激酶和己糖激酶没有影响,这表明这种ATP类似物是所谓“P型”ATP酶的特异性失活剂。

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