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Rab5b 相关的 Arf1 GTP 酶调节 N-豆蔻酰化腺苷酸激酶 2 从内质网的输出。

Rab5b-Associated Arf1 GTPase Regulates Export of N-Myristoylated Adenylate Kinase 2 From the Endoplasmic Reticulum in .

机构信息

Department of Parasitology, National Institute of Infectious Diseases, Tokyo, Japan.

Graduate School of Life and Environmental Sciences, University of Tsukuba, Ibaraki, Japan.

出版信息

Front Cell Infect Microbiol. 2021 Feb 2;10:610200. doi: 10.3389/fcimb.2020.610200. eCollection 2020.

Abstract

extensively remodels human erythrocytes by exporting hundreds of parasite proteins. This remodeling is closely linked to the virulence-related functions and immune evasion. The N-terminal export signal named PEXEL ( export element) was identified to be important for the export of proteins beyond the PVM, however, the issue of how these PEXEL-positive proteins are transported and regulated by Rab GTPases from the endoplasmic reticulum (ER) to the cell surface has remained poorly understood. Previously, we identified new aspects of the trafficking of N-myristoylated adenylate kinase 2 (PfAK2), which lacks the PEXEL motif and is regulated by the PfRab5b GTPase. Overexpression of PfRab5b suppressed the transport of PfAK2 to the parasitophorous vacuole membrane and PfAK2 was accumulated in the punctate compartment within the parasite. Here, we report the identification of PfRab5b associated proteins and dissect the pathway regulated by PfRab5b. We isolated two membrane trafficking GTPases PfArf1 and PfRab1b by coimmunoprecipitation with PfRab5b and mass analysis. PfArf1 and PfRab1b are both colocalized with PfRab5b adjacent to the ER in the early erythrocytic stage. A super-resolution microgram of the indirect immunofluorescence assay using PfArf1 or PfRab1b- expressing parasites revealed that PfArf1 and PfRab1b are localized to different ER subdomains. We used a genetic approach to expresses an active or inactive mutant of PfArf1 that specifically inhibited the trafficking of PfAK2 to the parasitophorous vacuole membrane. While expression of PfRab1b mutants did not affect in the PfAK2 transport. In contrast, the export of the PEXEL-positive protein Rifin was decreased by the expression of the inactive mutant of PfRab1b or PfArf1. These data indicate that the transport of PfAK2 and Rifin were recognized at the different ER subdomain by the two independent GTPases: PfAK2 is sorted by PfArf1 into the pathway for the PV, and the export of Rifin might be sequentially regulated by PfArf1 and PfRab1b.

摘要

疟原虫通过输出数百种寄生虫蛋白对人类红细胞进行广泛重塑。这种重塑与毒力相关功能和免疫逃避密切相关。已确定 N 端输出信号(称为 PEXEL(出口元件))对于将蛋白输出到 PVM 之外很重要,然而,这些 PEXEL 阳性蛋白如何通过内质网 (ER) 中的 Rab GTPase 运输和调节到细胞表面的问题仍知之甚少。以前,我们确定了 N-豆蔻酰化腺苷酸激酶 2 (PfAK2) 运输的新方面,PfAK2 缺乏 PEXEL 基序并受 PfRab5b GTPase 调节。PfRab5b 的过表达抑制了 PfAK2 向寄生空泡膜的运输,PfAK2 在寄生虫内的点状隔室内积累。在这里,我们报告了 PfRab5b 相关蛋白的鉴定,并剖析了 PfRab5b 调节的途径。我们通过与 PfRab5b 共免疫沉淀和质谱分析分离了两种膜转运 GTPase PfArf1 和 PfRab1b。PfArf1 和 PfRab1b 在红细胞早期阶段与 PfRab5b 一起在 ER 附近共定位。使用 PfArf1 或 PfRab1b 表达寄生虫的间接免疫荧光测定的超分辨率显微术显示,PfArf1 和 PfRab1b 定位于不同的 ER 亚区。我们使用遗传方法表达了一种活性或非活性突变体 PfArf1,该突变体专门抑制 PfAK2 向寄生空泡膜的运输。虽然 PfRab1b 突变体的表达不影响 PfAK2 的运输。相比之下,PEXEL 阳性蛋白 Rifin 的表达减少了 PfRab1b 或 PfArf1 的不活性突变体的表达。这些数据表明 PfAK2 和 Rifin 的运输是由两种独立的 GTPase 在不同的 ER 亚区识别的:PfAK2 由 PfArf1 分选到 PV 途径,而 Rifin 的出口可能依次受 PfArf1 和 PfRab1b 调节。

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