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真核起始因子 2α 激酶的小分子调节剂,是蛋白质合成的关键调节因子。

Small molecule modulators of eukaryotic initiation factor 2α kinases, the key regulators of protein synthesis.

机构信息

Bioinformatics Center, University of Pune, Pune - 411007, Maharashtra, India.

出版信息

Biochimie. 2013 Nov;95(11):1980-90. doi: 10.1016/j.biochi.2013.07.030. Epub 2013 Aug 11.

DOI:10.1016/j.biochi.2013.07.030
PMID:23939221
Abstract

Eukaryotic initiation factor 2 alpha kinases (eIF-2α kinases) are key mediators of stress response in cells. In mammalian cells, there are four eIF-2α kinases, namely HRI (Heme-Regulated Inhibitor), PKR (RNA-dependent Protein Kinase), PERK (PKR-like ER Kinase) and GCN2 (General Control Non-derepressible 2). These kinases get activated during diverse cytoplasmic stress conditions and phosphorylate the alpha-subunit of eIF2, leading to global protein synthesis inhibition. Therefore, eIF-2α kinases play a vital role in various cellular processes such as proliferation, differentiation, apoptosis and cell signaling. Deregulation of eIF-2α kinases and protein synthesis has been linked to numerous pathological conditions such as certain cancers, anemia and neurodegenerative disorders. Thus, modulation of these kinases by small molecules holds a great therapeutic promise. In this review we have compiled the available information on inhibitors and activators of these four eIF-2α kinases. The review concludes with a note on the selectivity issue of currently available modulators and future perspectives for the design of specific small molecule probes.

摘要

真核起始因子 2α 激酶(eIF-2α kinases)是细胞应激反应的关键介质。在哺乳动物细胞中,有四种 eIF-2α 激酶,分别是 HRI(血红素调节抑制剂)、PKR(RNA 依赖性蛋白激酶)、PERK(PKR 样内质网激酶)和 GCN2(一般控制非阻遏物 2)。这些激酶在各种细胞质应激条件下被激活,磷酸化 eIF2 的α 亚基,导致全局蛋白质合成抑制。因此,eIF-2α 激酶在细胞增殖、分化、凋亡和细胞信号转导等多种细胞过程中发挥着重要作用。eIF-2α 激酶和蛋白质合成的失调与许多病理状况有关,如某些癌症、贫血和神经退行性疾病。因此,小分子对这些激酶的调节具有很大的治疗潜力。在这篇综述中,我们汇集了关于这四种 eIF-2α 激酶的抑制剂和激活剂的现有信息。综述最后还提到了目前可用调节剂的选择性问题以及设计特异性小分子探针的未来展望。

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