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过氧化物酶体蛋白输入机制的外周成分Pex17p的Pex19p依赖性靶向作用。

Pex19p-dependent targeting of Pex17p, a peripheral component of the peroxisomal protein import machinery.

作者信息

Girzalsky Wolfgang, Hoffmann Linda S, Schemenewitz Andreas, Nolte Andreas, Kunau Wolf-Hubert, Erdmann Ralf

机构信息

Abteilung für Systembiochemie, Institut für Physiologische Chemie, Ruhr-Universität Bochum, D-44780 Bochum, Germany.

出版信息

J Biol Chem. 2006 Jul 14;281(28):19417-25. doi: 10.1074/jbc.M603344200. Epub 2006 May 4.

Abstract

Pex19p is required for the topogenesis of peroxisomal membrane proteins (PMPs). Here we have demonstrated that Pex19p is also required for the peroxisomal targeting and stability of Pex17p, a peripheral component of the docking complex of the peroxisomal protein import machinery. We have demonstrated that Pex17p is associated with the peroxisomal Pex13p-Pex14p complex as well as with Pex19p. We have identified the corresponding binding sites for Pex14p and Pex19p and demonstrated that a specific loss of the Pex19p interaction resulted in mistargeting of Pex17p. We have shown that a construct consisting only of the Pex19p- and Pex14p-binding sites of Pex17p is sufficient to direct an otherwise cytosolic reporter protein to the peroxisomal membrane in a Pex19p-dependent manner. Our data show that the function of Pex19p as chaperone or import receptor is not restricted to integral membrane proteins but may also include peripheral PMPs. As a consequence of our data, the previous definition of a targeting signal for PMPs (mPTS) as a Pex19p-binding motif in conjunction with a transmembrane segment should be extended to regions comprising a Pex19p-binding motif and a peroxisomal anchor sequence.

摘要

过氧化物酶体膜蛋白(PMPs)的拓扑结构形成需要Pex19p。在此我们证明,过氧化物酶体蛋白导入机制对接复合物的外周成分Pex17p的过氧化物酶体靶向和稳定性也需要Pex19p。我们已证明Pex17p与过氧化物酶体的Pex13p - Pex14p复合物以及Pex19p相关联。我们已确定了Pex14p和Pex19p的相应结合位点,并证明Pex19p相互作用的特异性丧失会导致Pex17p靶向错误。我们已表明,仅由Pex17p的Pex19p和Pex14p结合位点组成的构建体足以以依赖Pex19p的方式将原本位于胞质中的报告蛋白导向过氧化物酶体膜。我们的数据表明,Pex19p作为伴侣蛋白或导入受体的功能不仅限于整合膜蛋白,还可能包括外周PMPs。基于我们的数据,之前将PMPs的靶向信号(mPTS)定义为与跨膜区段结合的Pex19p结合基序,应扩展至包含Pex19p结合基序和过氧化物酶体锚定序列的区域。

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