Department of Microbiology and Immunology, Stanford School of Medicine, Stanford California, USA.
Broad Institutegrid.66859.34 of MIT and Harvard, Cambridge, Massachusetts, USA.
mBio. 2021 Dec 21;12(6):e0026021. doi: 10.1128/mBio.00260-21. Epub 2021 Nov 9.
Toxoplasma gondii is a ubiquitous, intracellular parasite that envelops its parasitophorous vacuole with a protein-laden membrane (PVM). The PVM is critical for interactions with the infected host cell, such as nutrient transport and immune defense. Only a few parasite and host proteins have so far been identified on the host-cytosolic side of the PVM. We report here the use of human foreskin fibroblasts expressing the proximity-labeling enzyme miniTurbo, fused to a domain that targets it to this face of the PVM, in combination with quantitative proteomics to specifically identify proteins present at this interface. Out of numerous human and parasite proteins with candidate PVM localization, we validate three parasite proteins (TGGT1_269950 [GRA61], TGGT1_215360 [GRA62], and TGGT1_217530 [GRA63]) and four new host proteins (PDCD6IP/ALIX, PDCD6, CC2D1A, and MOSPD2) as localized to the PVM in infected human cells through immunofluorescence microscopy. These results significantly expand our knowledge of proteins present at the PVM and, given that three of the validated host proteins are components of the ESCRT (endosomal sorting complexes required for transport) machinery, they further suggest that novel biology is operating at this crucial host-pathogen interface. is an intracellular pathogen which resides and replicates inside a membrane-bound vacuole in infected cells. This vacuole is modified by both parasite and host proteins which participate in a variety of host-parasite interactions at this interface, including nutrient exchange, effector transport, and immune modulation. Only a small number of parasite and host proteins present at the vacuolar membrane and exposed to the host cytosol have thus far been identified. Here, we report the identification of several novel parasite and host proteins present at the vacuolar membrane using enzyme-catalyzed proximity-labeling, significantly increasing our knowledge of the molecular players present and novel biology occurring at this crucial interface.
刚地弓形虫是一种普遍存在的细胞内寄生虫,它用富含蛋白质的膜(PVM)包裹其寄生空泡。PVM 对于与感染宿主细胞的相互作用至关重要,例如营养物质运输和免疫防御。迄今为止,只有少数寄生虫和宿主蛋白被鉴定为 PVM 宿主细胞质侧的蛋白。我们在此报告使用表达邻近标记酶 miniTurbo 的人包皮成纤维细胞,该酶融合到一个将其靶向 PVM 此面的结构域,结合定量蛋白质组学来特异性鉴定存在于该界面的蛋白质。在具有候选 PVM 定位的众多人类和寄生虫蛋白中,我们验证了三种寄生虫蛋白(TGGT1_269950[GRA61]、TGGT1_215360[GRA62]和 TGGT1_217530[GRA63])和四种新的宿主蛋白(PDCD6IP/ALIX、PDCD6、CC2D1A 和 MOSPD2)作为定位于感染人细胞中的 PVM 的蛋白通过免疫荧光显微镜。这些结果显著扩展了我们对 PVM 中存在的蛋白质的了解,并且鉴于验证的三种宿主蛋白是 ESCRT(内体分选复合物所需的运输)机制的组成部分,它们进一步表明在这个关键的宿主-病原体界面上存在新的生物学。 是一种细胞内病原体,它存在于感染细胞的膜结合空泡中并在其中复制。这个空泡被寄生虫和宿主蛋白修饰,它们在这个界面参与各种宿主-寄生虫相互作用,包括营养物质交换、效应物运输和免疫调节。迄今为止,只有少数存在于空泡膜上并暴露于宿主细胞质中的寄生虫和宿主蛋白被鉴定出来。在这里,我们报告了使用酶催化邻近标记法鉴定存在于空泡膜上的几种新的寄生虫和宿主蛋白,这显著增加了我们对存在于该关键界面的分子成分和新生物学的了解。