Paredes Franco Jose Carlos, Sampaio Guther Maria Lucia, Lima Marta L, Ferguson Michael A J
Wellcome Centre for Anti-Infectives Research, Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee DD1 5HN, United Kingdom.
Wellcome Centre for Anti-Infectives Research, Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee DD1 5HN, United Kingdom.
Mol Biochem Parasitol. 2023 Dec;256:111590. doi: 10.1016/j.molbiopara.2023.111590. Epub 2023 Aug 29.
Previous work has shown that the TbFUT1 and LmjFUT1 genes encode essential fucosyltransferases located inside the single mitochondria of the protozoan parasites Trypanosoma brucei and Leishmania major, respectively. However, nothing was known about the orthologous gene TcFUT1 or its gene product in Trypanosoma cruzi, aetiological agent of Chagas disease. In this study, we describe the overexpression of TcFUT1 with a C-terminal 6xMyc epitope tag in T. cruzi epimastigote cells. Overexpressed and immunoprecipitated TcFUT1-6xMyc was used to demonstrate enzymatic activity and to explore substrate specificity. This defined TcFUT1 as a GDP-Fuc : βGal α1-2 fucosyltransferase with a strict requirement for acceptor glycans with non-reducing terminal Galβ1-3GlcNAc structures. This differs from the specificity of the T. brucei orthologue TbFUT1, which can also tolerate non-reducing terminal Galβ1-4GlcNAc and Galβ1-4Glc acceptor sites. Immunofluorescence microscopy using α-Myc tag antibodies also showed a mitochondrial location for TcFUT1 in T. cruzi epimastigote cells. Collectively, these results are like those described for TbFUT1 and LmjFUT1 from T. brucei and L. major, suggesting that FUT1 gene products have conserved function for across the trypanosomatids and may share therapeutic target potential.
先前的研究表明,TbFUT1和LmjFUT1基因分别编码位于原生动物寄生虫布氏锥虫和硕大利什曼原虫单个线粒体内的必需岩藻糖基转移酶。然而,对于恰加斯病的病原体克氏锥虫中的直系同源基因TcFUT1或其基因产物却一无所知。在本研究中,我们描述了在克氏锥虫前鞭毛体细胞中C端带有6xMyc表位标签的TcFUT1的过表达。过表达并免疫沉淀的TcFUT1-6xMyc用于证明酶活性并探索底物特异性。这确定TcFUT1为一种GDP-岩藻糖:β-半乳糖α1-2岩藻糖基转移酶,对具有非还原末端Galβ1-3GlcNAc结构的受体聚糖有严格要求。这与布氏锥虫直系同源物TbFUT1的特异性不同,后者也可以耐受非还原末端Galβ1-4GlcNAc和Galβ1-4Glc受体位点。使用α-Myc标签抗体的免疫荧光显微镜检查也显示TcFUT1在克氏锥虫前鞭毛体细胞中的线粒体定位。总体而言,这些结果与布氏锥虫和硕大利什曼原虫中TbFUT1和LmjFUT1的描述相似,表明FUT1基因产物在整个锥虫中具有保守功能,并且可能具有共同的治疗靶点潜力。