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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >The peroxisomal import receptor PEX5 functions as a stress sensor, retaining catalase in the cytosol in times of oxidative stress
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The peroxisomal import receptor PEX5 functions as a stress sensor, retaining catalase in the cytosol in times of oxidative stress

机译:过氧缩样进口受体PEX5用作应力传感器,在氧化应激的时间内保持胞嘧啶中的过氧化氢酶

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Abstract Accumulating evidence indicates that peroxisome functioning, catalase localization, and cellular oxidative balance are intimately interconnected. Nevertheless, it remains largely unclear why modest increases in the cellular redox state especially interfere with the subcellular localization of catalase, the most abundant peroxisomal antioxidant enzyme. This study aimed at gaining more insight into this phenomenon. Therefore, we first established a simple and powerful approach to study peroxisomal protein import and protein-protein interactions in living cells in response to changes in redox state. By employing this approach, we confirm and extend previous observations that Cys-11 of human PEX5, the shuttling import receptor for peroxisomal matrix proteins containing a C-terminal peroxisomal targeting signal (PTS1), functions as a redox switch that modulates the protein's activity in response to intracellular oxidative stress. In addition, we show that oxidative stress affects the import of catalase, a non-canonical PTS1-containing protein, more than the import of a reporter protein containing a canonical PTS1. Furthermore, we demonstrate that changes in the local redox state do not affect PEX5-substrate binding and that human PEX5 does not oligomerize in cellulo , not even when the cells are exposed to oxidative stress. Finally, we present evidence that catalase retained in the cytosol can protect against H 2 O 2 -mediated redox changes in a manner that peroxisomally targeted catalase does not. Together, these findings lend credit to the idea that inefficient catalase import, when coupled with the role of PEX5 as a redox-regulated import receptor, constitutes a cellular defense mechanism to combat oxidative insults of extra-peroxisomal origin. Graphical abstract Display Omitted Highlights ? Alterations in cellular redox state do not affect PEX5 substrate binding. ? Redox changes differentially affect the import of different PTS1 proteins. ? Inefficient catalase import protects the cytosol against H 2 O 2 -induced insults. ]]>
机译:摘要累积证据表明过氧化物功能功能,过氧化酶定位和细胞氧化平衡密切相关。然而,它仍然很大程度上不清楚为什么适度增加细胞氧化还原状态,特别是干扰过氧化氢酶的亚细胞定位,最丰富的过氧化合物异体抗氧化酶。这项研究旨在获得对这种现象的更多洞察力。因此,我们首先建立了一种简单而强大的方法,以应对氧化还原状态的变化,研究活细胞的过氧异相蛋白质进口和蛋白质 - 蛋白质相互作用。通过采用这种方法,我们确认并延长了人Pex5的Cys-11,含有C末端过氧酶异构体靶向信号(PTS1)的过氧血清基质蛋白的穿梭进口受体,用作调节蛋白质的活性的氧化还原开关对细胞内氧化应激的反应。此外,我们表明氧化应激影响了过氧化氢酶的进口,含非规范PTS1的蛋白质,而不是含有规范PTS1的报告蛋白的进口。此外,我们证明局部氧化还原状态的变化不会影响PEX5-底物结合,并且即使细胞暴露于氧化应激时,人Pex5也不会在纤维素中脱极化。最后,我们提出了证据,即保留在胞质溶胶中的过氧化氢酶可以以过氧血征靶向过氧氢酶不存在的方式保护H 2 O介导的氧化还原变化。这些发现在一起借给效率低低于过氧化氢进口受体的过滤酶导入的效率的理念,构成了对抗超异甲虫异种体重血清血症的氧化损伤的细胞防御机制。图形抽象显示省略了亮点?细胞氧化还原状态的改变不会影响PEX5底物结合。还氧化还原变化差异地影响了不同的PTS1蛋白的导入。还低效的过氧化氢酶进口保护细胞溶溶胶免受H 2 O 2诱导的损伤。 ]]>

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