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阴道毛滴虫滋养体和假囊的深入定量蛋白质组分析。

In-Depth Quantitative Proteomic Analysis of Trophozoites and Pseudocysts of Trichomonas vaginalis.

机构信息

Department of Proteomics and Signal Transduction , Max-Planck-Institute for Biochemistry , 82152 Martinsried , Germany.

Departamento de Medicina , Universidade Federal de São João del Rei , 36301-160 São João del Rei , Minas Gerais Brazil.

出版信息

J Proteome Res. 2018 Nov 2;17(11):3704-3718. doi: 10.1021/acs.jproteome.8b00343. Epub 2018 Oct 3.

Abstract

Trichomonas vaginalis is a sexually transmitted anaerobic parasite that infects humans causing trichomoniasis, a common and ubiquitous sexually transmitted disease. The life cycle of this parasite possesses a trophozoite form without a cystic stage. However, the presence of nonproliferative and nonmotile, yet viable and reversible spherical forms with internalized flagella, denominated pseudocysts, has been commonly observed for this parasite. To understand the mechanisms involved in the formation of pseudocysts, we performed a mass spectrometry-based high-throughput quantitative proteomics study using a label-free approach and functional assays by biochemical and flow cytometric methods. We observed that the morphological transformation of trophozoite to pseudocysts is coupled to (i) a metabolic shift toward a less glycolytic phenotype; (ii) alterations in the abundance of hydrogenosomal iron-sulfur cluster (ISC) assembly machinery; (iii) increased abundance of regulatory particles of the ubiquitin-proteasome system; (iv) significant alterations in proteins involved in adhesion and cytoskeleton reorganization; and (v) arrest in G2/M phase associated with alterations in the abundance of regulatory proteins of the cell cycle. These data demonstrate that pseudocysts experience important physiological and structural alterations for survival under unfavorable environmental conditions.

摘要

阴道毛滴虫是一种性传播的厌氧寄生虫,感染人类会导致滴虫病,这是一种常见且普遍存在的性传播疾病。这种寄生虫的生命周期没有囊泡阶段,只有滋养体形式。然而,通常可以观察到这种寄生虫存在非增殖和非运动的、但具有活力和可逆转的、内部有鞭毛的球形形式,称为假囊泡。为了了解形成假囊泡的机制,我们使用无标记方法和生化及流式细胞术等功能测定方法进行了基于质谱的高通量定量蛋白质组学研究。我们观察到,从滋养体到假囊泡的形态转化与以下几个方面有关:(i)代谢向低糖酵解表型的转变;(ii)氢化酶铁硫簇(ISC)组装机制丰度的改变;(iii)泛素-蛋白酶体系统调节颗粒的丰度增加;(iv)参与黏附和细胞骨架重排的蛋白质的显著改变;以及(v)与细胞周期调控蛋白丰度改变相关的 G2/M 期停滞。这些数据表明,假囊泡在不利的环境条件下为了生存经历了重要的生理和结构改变。

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