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蛋白酶体的漫游指南。

A hitchhiker's guide to the proteasome.

作者信息

von Arnim A G

机构信息

Department of Botany, University of Tennessee, Knoxville, TN 37996-1100, USA.

出版信息

Sci STKE. 2001 Aug 28;2001(97):pe2. doi: 10.1126/stke.2001.97.pe2.

Abstract

Regulated degradation of proteins is essential for viability and is involved in the control of many signal transduction pathways. von Arnim discusses a new model for how substrates destined for degradation by the 26S proteasome may be presented to the proteasome through a physical interaction between the proteasome and a complex consisting of the substrate and a ubiquitin-ligase. The new model suggests that the SCF (Skp1/cullin/F-box) protein complex may physically associate with the proteasome and that this interaction may be regulated by posttranslational modifications, such as phosphorylation or the covalent attachment of the Nedd8 protein, called neddylation. Additionally, other proteins may compete with the SCF complexes for binding to the proteasome and thus present another layer of regulation for controlling substrate targeting for ubiquitin-mediated degradation.

摘要

蛋白质的调控降解对细胞存活至关重要,且参与许多信号转导途径的控制。冯·阿尼姆讨论了一种新模型,该模型认为, destined for degradation by the 26S proteasome(此处表述有误,可能是“destined for degradation by the 26S proteasome”,即“ destined for degradation by the 26S proteasome”,即“被26S蛋白酶体降解的底物”)如何通过蛋白酶体与由底物和泛素连接酶组成的复合物之间的物理相互作用被呈递给蛋白酶体。新模型表明,SCF(Skp1/cullin/F-box)蛋白复合物可能与蛋白酶体发生物理结合,并且这种相互作用可能受翻译后修饰的调控,如磷酸化或Nedd8蛋白的共价连接(称为Neddylation)。此外,其他蛋白质可能会与SCF复合物竞争结合蛋白酶体,从而为控制泛素介导的降解底物靶向提供另一层调控。

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