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氧化型谷胱甘肽对蛋白质合成起始的抑制作用:一种使真核起始因子2的α亚基磷酸化的蛋白激酶的激活。

Inhibition of protein synthesis initiation by oxidized glutathione: activation of a protein kinase that phosphorylates the alpha subunit of eukaryotic initiation factor 2.

作者信息

Ernst V, Levin D H, London I M

出版信息

Proc Natl Acad Sci U S A. 1978 Sep;75(9):4110-4. doi: 10.1073/pnas.75.9.4110.

Abstract

Oxidized glutathione (GSSG) (0.02-0.5 mM) inhibits reticulocyte lysates by a mechanism similar to that observed in heme deficiency. Incubation of hemin-supplemented postribosomal supernates with GSSG results in the activation of a translational inhibitor [I(GSSG)]. The activation of I(GSSG) is enhanced by the presence of an energy-regenerating system. The simultaneous addition of 1 mM dithiothreitol blocks the activation of the GSSG-induced inhibitor; however, once inhibitor is formed, its activity is not affected by 1 mM dithiothreitol. GSSG-treated postribosomal supernates and partially purified preparations of I(GSSG) inhibit protein synthesis in hemin-supplemented lysates with biphasic kinetics. Inhibition by I(GSSG) is blocked by cyclic AMP (2-10 mM) and is potentiated by ATP (2 mM). The inhibition is also blocked or reversed by eukaryotic initiation factor eIF-2. The activation of I(GSSG) is accompanied by an increased cyclic AMP-independent protein kinase activity which phosphorylates the 38,000-dalton component (alpha subunit) of eIF-2; however, GSSG treatment of supernates does not alter the activity of the cyclic AMP-independent protein kinase activity that phosphorylates the 49,000-dalton polypeptide component (beta subunit) of eIF-2. These data indicate that GSSG treatment of reticulocyte lysates results in the activation of a protein kinase with inhibitory and phosphorylation properties similar to those of the heme-regulated cyclic AMP-independent protein kinase which is activated in heme deficiency.

摘要

氧化型谷胱甘肽(GSSG)(0.02 - 0.5 mM)通过一种类似于在血红素缺乏时观察到的机制抑制网织红细胞裂解物。用GSSG孵育添加了血红素的核糖体后上清液会导致一种翻译抑制剂[I(GSSG)]的激活。能量再生系统的存在会增强I(GSSG)的激活。同时添加1 mM二硫苏糖醇可阻断GSSG诱导的抑制剂的激活;然而,一旦抑制剂形成,其活性不受1 mM二硫苏糖醇的影响。经GSSG处理的核糖体后上清液和I(GSSG)的部分纯化制剂以双相动力学抑制添加了血红素的裂解物中的蛋白质合成。I(GSSG)的抑制作用被环磷酸腺苷(2 - 10 mM)阻断,并被ATP(2 mM)增强。这种抑制作用也被真核起始因子eIF - 2阻断或逆转。I(GSSG)的激活伴随着环磷酸腺苷非依赖性蛋白激酶活性的增加,该酶可使eIF - 2的38,000道尔顿组分(α亚基)磷酸化;然而,用GSSG处理上清液不会改变使eIF - 2的49,000道尔顿多肽组分(β亚基)磷酸化的环磷酸腺苷非依赖性蛋白激酶的活性。这些数据表明,用GSSG处理网织红细胞裂解物会导致一种蛋白激酶的激活,其抑制和磷酸化特性类似于在血红素缺乏时被激活的血红素调节的环磷酸腺苷非依赖性蛋白激酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75a8/336061/06cb16404993/pnas00668-0050-a.jpg

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