克鲁兹锥虫线粒体岩藻糖基转移酶TcFUT1的特性研究

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jose Carlos Paredes Franco, Maria Lucia Sampaio Guther, Marta L. Lima, Michael A.J. Ferguson
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引用次数: 0

摘要

先前的工作表明,TbFUT1和LmjFUT1基因编码的必需岩藻糖基转移酶分别位于原生动物寄生虫布氏锥虫和大利什曼原虫的单个线粒体内。然而,对Chagas病的病原体克鲁兹锥虫的同源基因TcFUT1或其基因产物一无所知。在这项研究中,我们描述了具有C末端6xMyc表位标签的TcFUT1在克鲁兹差向astigote细胞中的过表达。过度表达和免疫沉淀的TcFUT1–6xMyc用于证明酶活性和探索底物特异性。这将TcFUT1定义为一种GDP-Fuc:βGalα1–2岩藻糖基转移酶,对具有非还原性末端Galβ1–3GlcNAc结构的受体聚糖有严格要求。这与布鲁氏菌直系同源物TbFUT1的特异性不同,后者也可以耐受非还原性末端Galβ1-4GlcNAc和Galβ1-4 Glc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了克鲁兹曲霉菌差向astigote细胞中TcFUT1的线粒体位置。总之,这些结果与布鲁氏菌和L.major的TbFUT1和LmjFUT1的结果相似,表明FUT1基因产物对所有锥虫类具有保守的功能,并可能共享治疗靶点潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterisation of TcFUT1, a mitochondrial fucosyltransferase from Trypanosoma cruzi

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.

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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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