首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins
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PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins

机译:PEX3在I类过氧化物酶体膜蛋白的导入中充当PEX19对接因子

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摘要

PEX19 is a chaperone and import receptor for newly synthesized, class I peroxisomal membrane proteins (PMPs). PEX19 binds these PMPs in the cytoplasm and delivers them to the peroxisome for subsequent insertion into the peroxisome membrane, indicating that there may be a PEX19 docking factor in the peroxisome membrane. Here we show that PEX3 is required for PEX19 to dock at peroxisomes, interacts specifically with the docking domain of PEX19, and is required for recruitment of the PEX19 docking domain to peroxisomes. PEX3 is also sufficient to dock PEX19 at heterologous organelles and binds PEX19 via a conserved motif that is essential for this docking activity and for PEX3 function in general. Not surprisingly, transient inhibition of PEX3 abrogates class I PMP import but has no effect on class II PMP import or peroxisomal matrix protein import. Taken together, these results suggest that PEX3 plays a selective, essential, and direct role in PMP import as a docking factor for PEX19.
机译:PEX19是新合成的I类过氧化物酶体膜蛋白(PMP)的伴侣和进口受体。 PEX19将这些PMP结合到细胞质中,然后将它们传递到过氧化物酶体中,随后插入到过氧化物酶体膜中,表明过氧化物酶体膜中可能存在PEX19对接因子。在这里,我们显示PEX19是PEX19停靠在过氧化物酶体上所必需的,它与PEX19的停靠域特别相互作用,并且是PEX19对接域募集到过氧化物酶体所必需的。 PEX3也足以将PEX19对接在异源细胞器上,并通过保守的基序与PEX19结合,该基序对于这种对接活动和PEX3的功能至关重要。毫不奇怪,PEX3的瞬时抑制取消了I类PMP的输入,但对II类PMP的输入或过氧化物酶体基质蛋白的输入没有影响。综上所述,这些结果表明,PEX3在PMP导入中作为PEX19的对接因子具有选择性,必要和直接的作用。

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