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靶向和非靶向蛋白质组学分析囊尾蚴寄生虫蛋白。

Targeted and non-targeted proteomics to characterize the parasite proteins of metacestodes.

机构信息

Institute of Parasitology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Graduate School for Cellular and Biomedical Sciences (GCB), University of Bern, Bern, Switzerland.

出版信息

Front Cell Infect Microbiol. 2023 May 30;13:1170763. doi: 10.3389/fcimb.2023.1170763. eCollection 2023.

Abstract

The larval stage of the cestode is the causative agent of alveolar echinococcosis. To investigate the biology of these stages and to test novel compounds, metacestode cultures represent a suitable model system. These metacestodes are vesicles surrounded by an envelope formed by the vesicle tissue (VT), which is formed by the laminated and germinal layer, and filled with vesicle fluid (VF). We analyzed the proteome of VF and VT by liquid chromatography tandem mass spectrometry (LC-MS/MS) and identified a total of 2,954 parasite proteins. The most abundant protein in VT was the expressed conserved protein encoded by EmuJ_000412500, followed by the antigen B subunit AgB8/3a encoded by EmuJ_000381500 and Endophilin B1 (protein p29). In VF, the pattern was different and dominated by AgB subunits. The most abundant protein was the AgB8/3a subunit followed by three other AgB subunits. In total, the AgB subunits detected in VF represented 62.1% of the parasite proteins. In culture media (CM), 63 proteins were detected, of which AgB subunits made up 93.7% of the detected parasite proteins. All AgB subunits detected in VF (encoded by EmuJ_000381100-700, corresponding to AgB8/2, AgB8/1, AgB8/4, AgB8/3a, AgB8/3b, and AgB8/3c) were also found in CM, except the subunit encoded by EmuJ_000381800 (AgB8/5) that was very rare in VF and not detected in CM. The relative abundance of the AgB subunits in VF and CM followed the same pattern. In VT, only the subunits EmuJ_000381500 (AgB8/3a) and EmuJ_000381200 (AgB8/1) were detected among the 20 most abundant proteins. To see whether this pattern was specific to VF from cultured metacestodes, we analyzed the proteome of VF from metacestodes grown in a mouse model. Here, the AgB subunits encoded by EmuJ_000381100-700 constituted the most abundant proteins, namely, 81.9% of total protein, with the same order of abundance as . Immunofluorescence on metacestodes showed that AgB is co-localized to calcareous corpuscles of . Using targeted proteomics with HA-tagged EmuJ_000381200 (AgB8/1) and EmuJ_000381100 (AgB8/2), we could show that uptake of AgB subunits from CM into VF occurs within hours.

摘要

绦虫的幼虫阶段是泡型包虫病的病原体。为了研究这些阶段的生物学特性并测试新的化合物,囊尾蚴培养物是一种合适的模型系统。这些囊尾蚴是由囊泡组织(VT)包围的囊泡,由囊泡组织(VT)形成,由层状和生发层形成,并充满囊泡液(VF)。我们通过液相色谱串联质谱法(LC-MS/MS)分析了 VF 和 VT 的蛋白质组,共鉴定出 2954 种寄生虫蛋白。VT 中最丰富的蛋白是 EmuJ_000412500 编码的表达保守蛋白,其次是 EmuJ_000381500 编码的抗原 B 亚单位 AgB8/3a 和内收蛋白 B1(蛋白 p29)。在 VF 中,模式则不同,AgB 亚单位占主导地位。最丰富的蛋白是 AgB8/3a 亚单位,其次是另外三个 AgB 亚单位。总共,在 VF 中检测到的 AgB 亚单位占寄生虫蛋白的 62.1%。在培养基(CM)中,检测到 63 种蛋白,其中 AgB 亚单位占检测到的寄生虫蛋白的 93.7%。在 VF 中检测到的所有 AgB 亚单位(由 EmuJ_000381100-700 编码,对应 AgB8/2、AgB8/1、AgB8/4、AgB8/3a、AgB8/3b 和 AgB8/3c)也存在于 CM 中,除了由 EmuJ_000381800 编码的亚单位(AgB8/5)外,该亚单位在 VF 中非常罕见,在 CM 中未检测到。VF 和 CM 中 AgB 亚单位的相对丰度遵循相同的模式。在 VT 中,在 20 种最丰富的蛋白中,仅检测到 EmuJ_000381500(AgB8/3a)和 EmuJ_000381200(AgB8/1)这两个亚单位。为了观察这种模式是否是培养的囊尾蚴的 VF 所特有,我们分析了在小鼠模型中生长的囊尾蚴的 VF 蛋白质组。在这里,由 EmuJ_000381100-700 编码的 AgB 亚单位构成了最丰富的蛋白,即占总蛋白的 81.9%,其丰度顺序与 VF 相同。对囊尾蚴的免疫荧光染色显示,AgB 与棘球蚴的钙质体共定位。使用针对 HA 标记的 EmuJ_000381200(AgB8/1)和 EmuJ_000381100(AgB8/2)的靶向蛋白质组学,我们可以证明 AgB 亚单位从 CM 摄取到 VF 发生在数小时内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194c/10266102/32ca318b714f/fcimb-13-1170763-g001.jpg

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