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真核起始因子2α亚基部分磷酸化介导的翻译控制机制

Mechanism of translational control by partial phosphorylation of the alpha subunit of eukaryotic initiation factor 2.

作者信息

Siekierka J, Manne V, Ochoa S

出版信息

Proc Natl Acad Sci U S A. 1984 Jan;81(2):352-6. doi: 10.1073/pnas.81.2.352.

Abstract

Catalysis of ternary complex formation by the GDP exchange factor (GEF), in the presence of Mg2+, is blocked by phosphorylation of the alpha subunit of the eukaryotic initiation factor 2 (eIF-2). We proposed earlier that this phosphorylation interferes with the interaction between eIF-2 and GEF (then termed ESP). If so, inhibition should be related to the extent of phosphorylation. However, work in other laboratories indicated that in fully inhibited, heme-deficient lysates only 20-40% of the eIF-2 is phosphorylated. To understand the nature of the molecular lesion in eIF-2-alpha phosphorylation we used a system of pure components in which the rate of exchange of eIF-2-bound [3H]GDP with unlabeled GDP (via the reaction eIF-2-GDP + GEF in equilibrium eIF-2-GEF + GDP) was measured by using mixtures of eIF-2(alpha P) X [eH]GDP and eIF-2 X [3H]GDP in different proportions at constant concentration of eIF-2 X GEF. If, for example, the ratio of eIF-2 X GEF to total (phosphorylated and unphosphorylated) eIF-2 X [3H]GDP was 0.25, the exchange was found to be maximally inhibited when the proportion of eIF-2(alpha P) X [3H]GDP in hte mixture reached 25%. This suggests that the reaction stops because the available GEF is trapped in an inactive complex with eIF-2(alpha P). In the absence of free GEF, eIF-2 would not be able to recycle and initiation would come to a standstill when the available eIF-2 is tied up as eIF-2 X GDP. The trapping of GEF by eIF-s(alpha P) is strongly supported by the following observation. Incubation of eIF-2 X GEF with excess [3H]GDP leads to the formation of eIF-2 X [3H] GDP and free GEF and, if eIF-2(alpha 32P) X GDP is also present, all of the GEF is converted to eIF-2(alpha 32P) X GEF. This suggests that, whereas the equilibrium of the reaction eIF-2 X GEF + GDP in equilibrium eIF-2 X GDP + GEF favors the formation of free GEF, the equilibrium of the reaction eIF-2(alpha P) X GDP + GEF in equilibrium eIF-2(alpha P) X GEF + GDP is in favor of the association of GEF to eIF-2(alpha P).

摘要

在Mg2+存在的情况下,真核起始因子2(eIF-2)的α亚基发生磷酸化会阻断GDP交换因子(GEF)对三元复合物形成的催化作用。我们之前提出,这种磷酸化会干扰eIF-2与GEF之间的相互作用(当时称为ESP)。如果是这样,抑制作用应该与磷酸化程度相关。然而,其他实验室的研究表明,在完全抑制的、血红素缺乏的裂解物中,只有20%-40%的eIF-2发生了磷酸化。为了了解eIF-2-α磷酸化中分子损伤的本质,我们使用了一个纯组分系统,通过使用不同比例的eIF-2(αP)X[3H]GDP和eIF-2X[3H]GDP的混合物,在eIF-2XGEF浓度恒定的情况下,测量eIF-2结合的[3H]GDP与未标记GDP的交换速率(通过反应eIF-2-GDP + GEF⇌eIF-2-GEF + GDP)。例如,如果eIF-2XGEF与总(磷酸化和未磷酸化)eIF-2X[3H]GDP的比例为0.25,当混合物中eIF-2(αP)X[3H]GDP的比例达到25%时,发现交换受到最大程度的抑制。这表明反应停止是因为可用的GEF被困在与eIF-2(αP)的无活性复合物中。在没有游离GEF的情况下,eIF-2将无法循环利用,当可用的eIF-2以eIF-2XGDP的形式被束缚时,起始过程将停滞。eIF-s(αP)对GEF的捕获得到了以下观察结果的有力支持。将eIF-2XGEF与过量的[3H]GDP一起孵育会导致形成eIF-2X[3H]GDP和游离GEF,并且,如果也存在eIF-2(α32P)XGDP,所有的GEF都会转化为eIF-2(α32P)XGEF。这表明,虽然反应eIF-2XGEF + GDP⇌eIF-2XGDP + GEF的平衡有利于游离GEF的形成,但反应eIF-2(αP)XGDP + GEF⇌eIF-2(αP)XGEF + GDP的平衡有利于GEF与eIF-2(αP)的结合。

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