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

O. Vassallo, S. Castelli, A. Biswas, S. Sengupta, P. Das, I. d’Annessa, F. Oteri, A. Leoni, P. Tagliatesta, H. Majumder, A. Desideri
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引用次数: 7

Abstract

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 � M) 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.
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共轭二十碳五烯酸(cEPA)抑制L. donovani拓扑异构酶i并对L. donovani Promastigotes具有抗增殖活性
共轭二十碳五烯酸抑制纯化的L. donovani拓扑异构酶I的松弛活性,其效率高于相应的人酶。酸性化合物在酶的三维结构上的对接表明,该配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)之间的大相互作用网络来稳定,这为其有效的抑制作用提供了解释。该酸对L. donovani promastigotes (EC50= 75 μ M)也有很强的抗原虫活性,而对小鼠巨噬细胞(IC50 = 2 μ M)没有作用。综上所示,多诺瓦氏乳酸菌拓扑异构酶I可以被认为是一个有趣的分子靶点,共轭二十碳五烯酸可以被考虑作为抗利什曼病的可能的先导化合物。
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