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蛋白质二硫键异构酶是硫氧还蛋白还原酶的底物,具有硫氧还蛋白样活性。

Protein disulfide-isomerase is a substrate for thioredoxin reductase and has thioredoxin-like activity.

作者信息

Lundström J, Holmgren A

机构信息

Department of Physiological Chemistry, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Biol Chem. 1990 Jun 5;265(16):9114-20.

PMID:2188973
Abstract

We have demonstrated that calf liver protein disulfide-isomerase (Mr 57,000) is a substrate for calf thymus thioredoxin reductase and catalyzes NADPH-dependent insulin disulfide reduction. This reaction can be used as a simple assay for protein disulfide-isomerase during purification in place of the classical method of reactivation of incorrectly oxidized ribonuclease A. Protein disulfide-isomerase contains two redox-active disulfides/molecule which were reduced by NADPH and calf thioredoxin reductase (Km approximately 35 microM). The isomerase was a poor substrate for NADPH and Escherichia coli thioredoxin reductase, but the addition of E. coli thioredoxin resulted in rapid reduction of two disulfides/molecule. Tryptophan fluorescence spectra were shown to monitor the redox state of protein disulfide-isomerase. Fluorescence measurements demonstrated that thioredoxin--(SH)2 reduced the disulfides of the isomerase and allowed the kinetics of the reaction to be followed; the reaction was also catalyzed by calf thioredoxin reductase. Equilibrium measurements showed that the apparent redox potential of the active site disulfide/dithiols of the thioredoxin domains of protein disulfide-isomerase was about 30 mV higher than the disulfide/dithiol of E. coli thioredoxin. Consistent with this, experiments using dithiothreitol or NADPH and thioredoxin reductase-dependent reduction and precipitation of insulin demonstrated differences between protein disulfide-isomerase and thioredoxin, thioredoxin being a better disulfide reductase but less efficient isomerase. Protein disulfide-isomerase is thus a high molecular weight member of the thioredoxin system, able to interact with both mammalian NADPH-thioredoxin reductase and reduced thioredoxin. This may be important for nascent protein disulfide formation and other thiol-dependent redox reactions in cells.

摘要

我们已证明,小牛肝蛋白二硫键异构酶(分子量57,000)是小牛胸腺硫氧还蛋白还原酶的底物,并催化依赖NADPH的胰岛素二硫键还原。该反应可作为蛋白质二硫键异构酶纯化过程中的一种简单检测方法,以替代经典的使错误氧化的核糖核酸酶A重新激活的方法。蛋白质二硫键异构酶每个分子含有两个具有氧化还原活性的二硫键,它们可被NADPH和小牛硫氧还蛋白还原酶还原(Km约为35 microM)。该异构酶对NADPH和大肠杆菌硫氧还蛋白还原酶而言是一种较差的底物,但添加大肠杆菌硫氧还蛋白会导致每个分子的两个二硫键迅速还原。已表明可用色氨酸荧光光谱监测蛋白质二硫键异构酶的氧化还原状态。荧光测量表明,硫氧还蛋白-(SH)2还原了异构酶的二硫键,并可追踪反应动力学;该反应也可由小牛硫氧还蛋白还原酶催化。平衡测量表明,蛋白质二硫键异构酶硫氧还蛋白结构域活性位点二硫键/二硫醇的表观氧化还原电位比大肠杆菌硫氧还蛋白的二硫键/二硫醇约高30 mV。与此一致的是,使用二硫苏糖醇或NADPH以及硫氧还蛋白还原酶依赖的胰岛素还原和沉淀实验表明,蛋白质二硫键异构酶与硫氧还蛋白之间存在差异,硫氧还蛋白是一种更好的二硫键还原酶,但作为异构酶效率较低。因此,蛋白质二硫键异构酶是硫氧还蛋白系统的一种高分子量成员,能够与哺乳动物NADPH - 硫氧还蛋白还原酶和还原型硫氧还蛋白相互作用。这对于细胞中新生蛋白质二硫键的形成以及其他依赖硫醇的氧化还原反应可能很重要。

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