Jasinski Gabriel, Salas-Sarduy Emir, Vega Daniel, Fabian Lucas, Martini María Florencia, Moglioni Albertina G
Cátedra de Química Medicinal, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, CABA, C1113AAD, Argentina; Instituto de la Química y el Metabolismo del Fármaco (IQUIMEFA), CONICET-Universidad de Buenos Aires, CABA, 1113, Argentina.
Instituto de Investigaciones Biotecnológicas "Dr. Rodolfo Ugalde" (IIBIO), CONICET-Universidad de San Martín (UNSAM), San Martín, Buenos Aires 1650, Argentina.
Bioorg Med Chem. 2022 May 1;61:116708. doi: 10.1016/j.bmc.2022.116708. Epub 2022 Mar 16.
The development of cruzipain inhibitors represents one of the most attractive challenges in the search for drugs for the treatment of Chagas disease. A recombinant form of this enzyme, cruzain, has been crystallized with numerous inhibitors, excluding thiosemicarbazones. These compounds have been established as potent inhibitors of cruzain, although there is very little data in the literature of thiosemicarbazones tested on cruzipain. In this work, we present the results of the evaluation of eleven thiosemicarbazones on cruzipain, isolated from T. cruzi epimastigotes, six of them previously evaluated on cruzain. For these latter, we studied through computational methods, the mode of interaction with the active site of cruzain and the contribution of geometric parameters to the possible mechanism of action involved in the observed inhibition. Finally, from some geometric parameters analyzed on modeled TSC-cruzain complexes, a semi-quantitative relationship was established that could explain the inhibitory activity of thiosemicarbazones on cruzipain, the enzyme actually present in the parasite.
克鲁兹蛋白酶抑制剂的研发是寻找治疗恰加斯病药物过程中最具吸引力的挑战之一。这种酶的重组形式——克鲁萨因,已与众多抑制剂结晶,硫代氨基脲除外。这些化合物已被确定为克鲁萨因的有效抑制剂,尽管在文献中关于在克鲁兹蛋白酶上测试硫代氨基脲的数据非常少。在这项工作中,我们展示了对从克氏锥虫前鞭毛体中分离出的克鲁兹蛋白酶进行11种硫代氨基脲评估的结果,其中6种之前已在克鲁萨因上进行过评估。对于后一种情况,我们通过计算方法研究了它们与克鲁萨因活性位点的相互作用模式以及几何参数对观察到的抑制作用所涉及的可能作用机制的贡献。最后,根据在模拟的硫代氨基脲-克鲁萨因复合物上分析的一些几何参数,建立了一种半定量关系,该关系可以解释硫代氨基脲对寄生虫中实际存在的酶——克鲁兹蛋白酶的抑制活性。