Meléndez-Hernández Mayra Gisela, Barrios María Luisa Labra, Orozco Esther, Luna-Arias Juan Pedro
Departmento de Biología Celular, Cinvestav-IPN, Av. IPN 2508, Col. Zacatenco CP07360, D. F. México, México.
BMC Microbiol. 2008 Dec 23;8:235. doi: 10.1186/1471-2180-8-235.
Entamoeba histolytica is a professional phagocytic cell where the vacuolar ATPase plays a key role. This enzyme is a multisubunit complex that regulates pH in many subcellular compartments, even in those that are not measurably acidic. It participates in a wide variety of cellular processes such as endocytosis, intracellular transport and membrane fusion. The presence of a vacuolar type H+-ATPase in E. histolytica trophozoites has been inferred previously from inhibition assays of its activity, the isolation of the Ehvma1 and Ehvma3 genes, and by proteomic analysis of purified phagosomes.
We report the isolation and characterization of the Ehvma2 gene, which encodes for the subunit B of the vacuolar ATPase. This polypeptide is a 55.3 kDa highly conserved protein with 34 to 80% identity to orthologous proteins from other species. Particularly, in silico studies showed that EhV-ATPase subunit B displays 78% identity and 90% similarity to its Dictyostelium ortholog. A 462 bp DNA fragment of the Ehvma2 gene was expressed in bacteria and recombinant polypeptide was used to raise mouse polyclonal antibodies. EhV-ATPase subunit B antibodies detected a 55 kDa band in whole cell extracts and in an enriched fraction of DNA-containing organelles named EhkOs. The V-ATPase subunit B was located by immunofluorescence and confocal microscopy in many vesicles, in phagosomes, plasma membrane and in EhkOs. We also identified the genes encoding for the majority of the V-ATPase subunits in the E. histolytica genome, and proposed a putative model for this proton pump.
We have isolated the Ehvma2 gene which encodes for the V-ATPase subunit B from the E. histolytica clone A. This gene has a 154 bp intron and encodes for a highly conserved polypeptide. Specific antibodies localized EhV-ATPase subunit B in many vesicles, phagosomes, plasma membrane and in EhkOs. Most of the orthologous genes encoding for the EhV-ATPase subunits were found in the E. histolytica genome, indicating the conserved nature of V-ATPase in this parasite.
溶组织内阿米巴是一种专业吞噬细胞,液泡型ATP酶在其中发挥关键作用。该酶是一种多亚基复合物,可调节许多亚细胞区室的pH值,即使在那些没有明显酸性的区室中也是如此。它参与多种细胞过程,如内吞作用、细胞内运输和膜融合。先前已通过其活性抑制试验、Ehvma1和Ehvma3基因的分离以及纯化吞噬体的蛋白质组分析推断出溶组织内阿米巴滋养体中存在液泡型H⁺-ATP酶。
我们报告了Ehvma2基因的分离和表征,该基因编码液泡型ATP酶的B亚基。该多肽是一种55.3 kDa的高度保守蛋白,与其他物种的直系同源蛋白具有34%至80%的同一性。特别是,计算机模拟研究表明,EhV-ATP酶B亚基与其盘基网柄菌直系同源物具有78%的同一性和90%的相似性。Ehvma2基因的一个462 bp DNA片段在细菌中表达,重组多肽用于制备小鼠多克隆抗体。EhV-ATP酶B亚基抗体在全细胞提取物和富含DNA的细胞器(称为EhkOs)的部分中检测到一条55 kDa的条带。通过免疫荧光和共聚焦显微镜观察,V-ATP酶B亚基位于许多囊泡、吞噬体、质膜和EhkOs中。我们还在溶组织内阿米巴基因组中鉴定了编码大多数V-ATP酶亚基的基因,并提出了该质子泵的推定模型。
我们从溶组织内阿米巴克隆A中分离出了编码V-ATP酶B亚基的Ehvma2基因。该基因有一个154 bp的内含子,编码一种高度保守的多肽。特异性抗体将EhV-ATP酶B亚基定位在许多囊泡、吞噬体、质膜和EhkOs中。在溶组织内阿米巴基因组中发现了大多数编码EhV-ATP酶亚基的直系同源基因,表明该寄生虫中V-ATP酶的保守性质。