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过氧化物酶体生物发生:Arf和衣被蛋白复合物可能参与其中的环节。

Peroxisome biogenesis: where Arf and coatomer might be involved.

作者信息

Lay Dorothee, Gorgas Karin, Just Wilhelm W

机构信息

Biochemie-Zentrum der Universität Heidelberg (BZH), Im Neuenheimer Feld 328D-69120 Heidelberg, Germany.

出版信息

Biochim Biophys Acta. 2006 Dec;1763(12):1678-87. doi: 10.1016/j.bbamcr.2006.08.036. Epub 2006 Aug 30.

Abstract

The present review summarizes recent observations on binding of Arf and COPI coat to isolated rat liver peroxisomes. The general structural and functional features of both Arf and coatomer were considered along with the requirements and dependencies of peroxisomal Arf and coatomer recruitment. Studies on the expression of mammalian Pex11 proteins, mainly Pex11alpha and Pex11beta, intimately related to the process of peroxisome proliferation, revealed a sequence of individual steps including organelle elongation/tubulation, formation of membrane and matrix protein patches segregating distinct proteins from each other, development of membrane constrictions and final membrane fission. Based on the similarities of the processes leading to cargo selection and concentration on Golgi membranes on the one hand and to the formation of peroxisomal protein patches on the other hand, an implication of Arf and COPI in distinct processes of peroxisomal proliferation is hypothesized. Alternatively, peroxisomal Arf/COPI might facilitate the formation of COPI-coated peroxisomal vesicles functioning in cargo transport and retrieval from peroxisomes to the ER. Recent observations suggesting transport of Pex3 and Pex19 during early steps of peroxisome biogenesis from the ER to peroxisomes inevitably propose such a retrieval mechanism, provided the ER to peroxisome pathway is based on transporting vesicles.

摘要

本综述总结了近期关于Arf和COPI衣被与分离的大鼠肝脏过氧化物酶体结合的观察结果。我们考虑了Arf和衣被蛋白复合物的一般结构和功能特征,以及过氧化物酶体Arf和衣被蛋白复合物募集的要求和依赖性。对主要与过氧化物酶体增殖过程密切相关的哺乳动物Pex11蛋白(主要是Pex11α和Pex11β)表达的研究揭示了一系列单独的步骤,包括细胞器伸长/成管、形成将不同蛋白质彼此分离的膜和基质蛋白斑块、膜缢缩的发展以及最终的膜分裂。基于一方面导致货物在高尔基体膜上选择和浓缩的过程与另一方面过氧化物酶体蛋白斑块形成过程的相似性,推测Arf和COPI在过氧化物酶体增殖的不同过程中发挥作用。或者,过氧化物酶体Arf/COPI可能促进形成COPI包被的过氧化物酶体囊泡,其在货物运输以及从过氧化物酶体到内质网的回收中发挥作用。最近的观察结果表明,在过氧化物酶体生物发生的早期阶段,Pex3和Pex19从内质网运输到过氧化物酶体,这不可避免地提出了这样一种回收机制,前提是内质网到过氧化物酶体的途径是基于运输囊泡的。

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