...
首页> 外文期刊>The Open Antimicrobial Agents Journal >Conjugated Eicosapentaenoic Acid (cEPA) Inhibits L. donovani TopoisomeraseI and has an Antiproliferative Activity Against L. donovani Promastigotes
【24h】

Conjugated Eicosapentaenoic Acid (cEPA) Inhibits L. donovani TopoisomeraseI and has an Antiproliferative Activity Against L. donovani Promastigotes

机译:共轭二十碳五烯酸(cEPA)抑制多诺尼乳杆菌拓扑异构酶I,并具有对多诺氏乳杆菌前鞭毛体的抗增殖活性

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Conjugated eicosapentaenoic acid inhibits the relaxation activity of purified L. donovani topoisomerase I, with an efficiency higher than that displayed by the corresponding human enzyme. Docking of the acid compound over the 3D structure of the enzyme shows that the complex is stabilized by a large network of interaction between the compound and many residues located in proximity of the active site, including the catalytic tyrosine 222, providing an explanation for its efficient inhibitory effect. The acid has also a strong antiprotozoal activity against L. donovani promastigotes ( EC50= 75 μM) whilst it has no effect against murine macrophages (IC50 ~ 2 mM). Taken together the results indicate that L. donovani topoisomerase I can be considered an interesting molecular target and that conjugated eicosapentaenoic acid can be taken in consideration as a possible lead compound against leishmaniasis.
机译:共轭二十碳五烯酸抑制纯化的多诺氏乳杆菌拓扑异构酶I的松弛活性,其效率高于相应的人类酶所显示的效率。酸化合物与酶的3D结构对接表明,该复合物通过化合物与位于活性位点附近的许多残基(包括催化酪氨酸222)之间的大型相互作用网络而稳定,这为其有效提供了解释抑制作用。该酸还具有针对多诺氏乳杆菌(L. donovani promastigotes)的强原生动物活性(EC50 = 75μM),而对鼠巨噬细胞没有任何作用(IC50〜2 mM)。综上所述,结果表明多诺尼乳杆菌拓扑异构酶I可以被认为是令人感兴趣的分子靶标,并且缀合的二十碳五烯酸可以被认为是对抗利什曼病的可能的先导化合物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号