Diaz Jenny R, Ramírez Cesar A, Nocua Paola A, Guzman Fanny, Requena José M, Puerta Concepción J
Laboratorio de Parasitología Molecular, Departamento de Microbiología, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.
Núcleo de Biotecnología Curauma (NBC), Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile.
PLoS One. 2018 Jan 5;13(1):e0190618. doi: 10.1371/journal.pone.0190618. eCollection 2018.
The increase of leishmaniasis cases worldwide and the emergence of Leishmania strains resistant to current treatments make necessary to find new therapeutic targets. Proteases are appealing drug targets because they play pivotal roles in facilitating parasite survival and promoting pathogenesis. Enzymes belonging to the dipeptidyl peptidase 3 (DPP3) group have been described in different organisms such as mammals, insects and yeast, in which these enzymes have been involved in both protein turnover and protection against oxidative damage. The aim of this work was to characterize the structure and function of the Leishmania braziliensis DPP3 (LbDPP3) protein as the first step to elucidate its suitability as a potential drug target. Sequence alignment showed 43% of identity between LbDPP3 and its human orthologous (hDPP3) enzyme. Although the modeled protein adopted a globally conserved three-dimensional (3D) structure, structural differences were found in the vicinity of the active site and the substrate binding-cleft. In addition, the Leishmania protein was expressed as a soluble recombinant protein and its kinetics parameters were determined using the z-Arginine-Arginine-AMC substrate. The LbDPP3 activity was maximal at pH values between 8.0-8.5. Interestingly, classical enzyme inhibitors such as the tynorphin and its derivative peptide IVYPW were found to actively inhibit the LbDPP3 activity. Moreover, these DPP3 inhibitors showed a detrimental effect upon parasite survival, decreasing the viability of promastigotes by up to 29%. Finally, it was observed that LbDPP3 was equally expressed along the in vitro differentiation from promastigotes to axenic amastigotes. In conclusion, these findings suggest that the L. brazileinsis DPP3 could be a promising drug target.
全球利什曼病病例的增加以及对当前治疗产生抗性的利什曼原虫菌株的出现,使得寻找新的治疗靶点变得必要。蛋白酶是有吸引力的药物靶点,因为它们在促进寄生虫存活和推动发病机制方面发挥着关键作用。属于二肽基肽酶3(DPP3)组的酶已在不同生物体中被描述,如哺乳动物、昆虫和酵母,在这些生物体中,这些酶参与了蛋白质周转和抗氧化损伤保护。这项工作的目的是表征巴西利什曼原虫DPP3(LbDPP3)蛋白的结构和功能,作为阐明其作为潜在药物靶点适用性的第一步。序列比对显示LbDPP3与其人类同源酶(hDPP3)之间有43%的同一性。尽管建模的蛋白质采用了全局保守的三维(3D)结构,但在活性位点和底物结合裂隙附近发现了结构差异。此外,利什曼原虫蛋白被表达为可溶性重组蛋白,并使用z - 精氨酸 - 精氨酸 - AMC底物测定其动力学参数。LbDPP3活性在pH值8.0 - 8.5之间最大。有趣的是,发现经典的酶抑制剂如强啡肽及其衍生物肽IVYPW能有效抑制LbDPP3活性。此外,这些DPP3抑制剂对寄生虫存活显示出有害作用,使前鞭毛体的活力降低多达29%。最后,观察到LbDPP3在体外从前鞭毛体向无共生体无鞭毛体分化过程中表达水平相同。总之,这些发现表明巴西利什曼原虫DPP3可能是一个有前景的药物靶点。