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Plakilactones from the marine sponge Plakinastrella mamillaris. discovery of a new class of marine ligands of peroxisome proliferator-activated receptor γ

机译:海洋海绵Plakinastrella mamillaris的Plakilactones。过氧化物酶体增殖物激活受体γ的新型海洋配体的发现

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摘要

In this paper we report the isolation and the molecular characterization of a new class of PPARγ ligands from the marine environment. Biochemical characterization of a library of 13 oxygenated polyketides isolated from the marine sponge Plakinastrella mamillaris allowed the discovery of gracilioether B and plakilactone C as selective PPARγ ligands in transactivation assays. Both agents covalently bind to the PPARγ ligand binding domain through a Michael addition reaction involving a protein cysteine residue and the α,β-unsaturated ketone in their side chains. Additionally, gracilioether C is a noncovalent agonist for PPARγ, and methyl esters 1 and 2 are noncovalent antagonists. Structural requirements for the interaction of these agents within the PPARγ ligand binding domain were obtained by docking analysis. Gracilioether B and plakilactone C regulate the expression of PPARγ-dependent genes in the liver and inhibit the generation of inflammatory mediators by macrophages.
机译:在本文中,我们报告了从海洋环境中分离出的新型PPARγ配体的分子特征。从海洋海绵Plakinastrella mamillaris分离出的13个氧化聚酮化合物文库的生化特征表明,在反式激活分析中发现了作为选择性PPARγ配体的松香醚B和吡内酯C。两种试剂通过迈克尔加成反应共价结合至PPARγ配体结合结构域,所述迈克尔加成反应涉及在其侧链中的蛋白质半胱氨酸残基和α,β-不饱和酮。另外,松香醚C是PPARγ的非共价激动剂,而甲酯1和2是非共价拮抗剂。通过对接分析获得了这些试剂在PPARγ配体结合域内相互作用的结构要求。 Gracilioether B和plakilactone C调节肝脏中PPARγ依赖性基因的表达,并抑制巨噬细胞产生炎症介质。

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