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The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes

机译:两孔通道TPC1是通过早期和再循环内体有效蛋白质加工所必需的

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摘要

Two-pore channels (TPCs) are localized in endo-lysosomal compartments and assumed to play an important role for vesicular fusion and endosomal trafficking. Recently, it has been shown that both TPC1 and 2 were required for host cell entry and pathogenicity of Ebola viruses. Here, we investigate the cellular function of TPC1 using protein toxins as model substrates for distinct endosomal processing routes. Toxin uptake and activation through early endosomes but not processing through other compartments were reduced in TPC1 knockout cells. Detailed co-localization studies with subcellular markers confirmed predominant localization of TPC1 to early and recycling endosomes. Proteomic analysis of native TPC1 channels finally identified direct interaction with a distinct set of syntaxins involved in fusion of intracellular vesicles. Together, our results demonstrate a general role of TPC1 for uptake and processing of proteins in early and recycling endosomes, likely by providing high local Ca2+ concentrations required for SNARE-mediated vesicle fusion.
机译:两孔通道(TPC)位于溶酶体内室,并假定在水泡融合和内体运输中起重要作用。近来,已经显示TPC1和2对于宿主细胞进入和埃博拉病毒的致病性都是必需的。在这里,我们调查TPC1的细胞功能,使用蛋白质毒素作为不同内体加工途径的模型底物。 TPC1基因敲除细胞减少了通过早期内体的毒素吸收和激活,但没有通过其他区室进行处理。与亚细胞标记物进行的详细的共定位研究证实,TPC1主要定位于早期和回收的内体。天然TPC1通道的蛋白质组学分析最终确定了与细胞内囊泡融合中涉及的一组不同语法素的直接相互作用。在一起,我们的结果表明TPC1在早期和循环体内的蛋白质摄取和加工中的一般作用,可能是通过提供SNARE介导的囊泡融合所需的高局部Ca 2 + 浓度来实现的。

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