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氯利索环肽:真核生物蛋白质合成的新型抑制剂。

Chlorolissoclimides: new inhibitors of eukaryotic protein synthesis.

作者信息

Robert Francis, Gao Hong Qing, Donia Marwa, Merrick William C, Hamann Mark T, Pelletier Jerry

机构信息

Department of Biochemistry, McGill University, Montreal, Quebec, Canada.

出版信息

RNA. 2006 May;12(5):717-25. doi: 10.1261/rna.2346806. Epub 2006 Mar 15.

Abstract

Lissoclimides are cytotoxic compounds produced by shell-less molluscs through chemical secretions to deter predators. Chlorinated lissoclimides were identified as the active component of a marine extract from Pleurobranchus forskalii found during a high-throughput screening campaign to characterize new protein synthesis inhibitors. It was demonstrated that these compounds inhibit protein synthesis in vitro, in extracts prepared from mammalian and plant cells, as well as in vivo against mammalian cells. Our results suggest that they block translation elongation by inhibiting translocation, leading to an accumulation of ribosomes on mRNA. These data provide a rationale for the cytotoxic nature of this class of small molecule natural products.

摘要

Lissoclimides是无壳软体动物通过化学分泌物产生的细胞毒性化合物,用于威慑捕食者。在一项旨在鉴定新型蛋白质合成抑制剂的高通量筛选活动中,氯化lissoclimides被确定为来自福氏侧鳃海蛞蝓(Pleurobranchus forskalii)的一种海洋提取物的活性成分。结果表明,这些化合物在体外、从哺乳动物和植物细胞制备的提取物中以及在体内对哺乳动物细胞均能抑制蛋白质合成。我们的结果表明,它们通过抑制易位来阻断翻译延伸,导致核糖体在mRNA上积累。这些数据为这类小分子天然产物的细胞毒性本质提供了理论依据。

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