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首页> 外文期刊>Molecular and Biochemical Parasitology >The microsporidian polar tube: evidence for a third polar tube protein (PTP3) in Encephalitozoon cuniculi.
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The microsporidian polar tube: evidence for a third polar tube protein (PTP3) in Encephalitozoon cuniculi.

机译:微孢子虫极管:钩状脑炎中存在第三极管蛋白(PTP3)的证据。

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摘要

The invasion strategy used by microsporidia is primarily related to spore germination. Small differentiated spores of these fungi-related parasites inject their contents into target cells through the lumen of a rapidly extruded polar tube, as a prerequisite to obligate intracellular development. Previous studies in Encephalitozoon species that infect mammals have identified two major antigenic polar tube proteins (PTP1 and PTP2) which are predicted to contribute to the high tensile strength of the polar tube via an assembly process dependent on disulfide linkages. By immunoscreening of a cDNA library, we found that a novel PTP is encoded by a single transcription unit (3990 bp) located on the chromosome XI of E. cuniculi. PTP3 is predicted to be synthesized as a 1256-amino acid precursor with a cleavable signal peptide. The mature protein lacks cysteine residue and its large acidic core is flanked by highly basic N- and C-terminal regions. Immunolocalization data indicated that PTP3 is involved in the sporoblast-to-spore polar tube biogenesis. A transcriptional up-regulation during sporogony is supported by a strong increase in the relative amount of Ecptp mRNAs within host cells sampled at late post-infection times. To begin to explore polar tube-associated protein interactions, spore proteins were extracted in the presence of SDS and dithiothreitol then incubated with a chemical cross-linker (DSP or sulfo-EGS). A large multimeric complex was formed and shown to contain PTP1, PTP2 and PTP3 with a few other proteins. PTP3 is hypothesized to play a role in the control of the polar tube extrusion as part of a specific response to ionic stimuli.
机译:微孢子虫使用的入侵策略主要与孢子萌发有关。这些真菌相关寄生虫的小分化孢子通过快速挤出的极管腔将其内含物注射到靶细胞中,这是进行细胞内发育的先决条件。先前对感染哺乳动物的脑袋虫物种的研究已经确定了两种主要的抗原性极管蛋白(PTP1和PTP2),据预测它们会通过依赖于二硫键的组装过程而对极管的高拉伸强度作出贡献。通过对cDNA文库的免疫筛选,我们发现一种新型的PTP由位于大肠杆菌的XI染色体上的单个转录单位(3990 bp)编码。预测PTP3可以合成为带有可裂解信号肽的1256-氨基酸前体。成熟的蛋白质缺乏半胱氨酸残基,其大的酸性核心位于高度碱性的N和C末端区域。免疫定位数据表明PTP3参与了孢子母细胞-孢子极管的生物发生。孢子形成期间的转录上调受到感染后后期采样的宿主细胞内Ecptp mRNA相对含量的强烈增加的支持。为了开始探索与极管相关的蛋白质相互作用,在SDS和二硫苏糖醇存在下提取孢子蛋白质,然后与化学交联剂(DSP或磺基-EGS)一起孵育。形成了一个大型的多聚体复合物,显示含有PTP1,PTP2和PTP3以及一些其他蛋白质。据推测,PTP3作为对离子刺激的特定反应的一部分,在控制极管挤出中发挥作用。

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