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Investigations on the mode of action of gephyronic acid an inhibitor of eukaryotic protein translation from myxobacteria

机译:粘菌真核蛋白翻译抑制剂gephyronic acid的作用方式研究

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摘要

The identification of inhibitors of eukaryotic protein biosynthesis, which are targeting single translation factors, is highly demanded. Here we report on a small molecule inhibitor, gephyronic acid, isolated from the myxobacterium Archangium gephyra that inhibits growth of transformed mammalian cell lines in the nM range. In direct comparison, primary human fibroblasts were shown to be less sensitive to toxic effects of gephyronic acid than cancer-derived cells. Gephyronic acid is targeting the protein translation system. Experiments with IRES dual luciferase reporter assays identified it as an inhibitor of the translation initiation. DARTs approaches, co-localization studies and pull-down assays indicate that the binding partner could be the eukaryotic initiation factor 2 subunit alpha (eIF2α). Gephyronic acid seems to have a different mode of action than the structurally related polyketides tedanolide, myriaporone, and pederin and is a valuable tool for investigating the eukaryotic translation system. Because cancer derived cells were found to be especially sensitive, gephyronic acid could potentially find use as a drug candidate.
机译:迫切需要鉴定靶向单翻译因子的真核生物合成抑制剂。在这里,我们报道了一种小分子抑制剂gephyronic acid,它从黏附细菌Archangium gephyra中分离出来,可抑制转化的哺乳动物细胞系在nM范围内的生长。直接比较,显示人类原代成纤维细胞对gephyronic acid的毒性作用不如源自癌症的细胞敏感。 Gephyronic酸靶向蛋白质翻译系统。使用IRES双重荧光素酶报告基因检测的实验将其鉴定为翻译起始的抑制剂。 DART方法,共定位研究和下拉测定法表明结合伴侣可能是真核起始因子2亚基α(eIF2α)。与结构相关的聚酮化合物泰达内酯,Myriaporone和pederin相比,Gephyronic酸似乎具有不同的作用方式,并且是研究真核翻译系统的有价值的工具。由于发现癌症细胞特别敏感,因此gephyronic acid可能会用作候选药物。

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