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肌动蛋白细胞骨架与小分子热休克蛋白:它们如何相互作用?

Actin cytoskeleton and small heat shock proteins: how do they interact?

作者信息

Mounier Nicole, Arrigo André-Patrick

机构信息

Laboratoire du Stress Oxydant, Chaperons et Apoptose, Centre de Génétique Moléculaire et Cellulaire (UMR-CNRS 5534), Université Claude Bernard Lyon1, Villeurbanne, France.

出版信息

Cell Stress Chaperones. 2002 Apr;7(2):167-76. doi: 10.1379/1466-1268(2002)007<0167:acashs>2.0.co;2.

Abstract

Actin and small heat shock proteins (sHsps) are ubiquitous and multifaceted proteins that exist in 2 reversible forms, monomers and multimers, ie, the microfilament of the cytoskeleton and oligomers of the sHsps, generally, supposed to be in a spherical and hollow form. Two situations are described in the literature, where the properties of actin are modulated by sHsps; the actin polymerization is inhibited in vitro by some sHsps acting as capping proteins, and the actin cytoskeleton is protected by some sHsps against the disruption induced by various stressful conditions. We propose that a direct actin-sHsp interaction occurs to inhibit actin polymerization and to participate in the in vivo regulation of actin filament dynamics. Protection of the actin cytoskeleton would result from an F-actin-sHsp interaction in which microfilaments would be coated by small oligomers of phosphorylated sHsps. Both proteins share common structural motives suggesting direct binding sites, but they remain to be demonstrated. Some sHsps would behave with the actin cytoskeleton as actin-binding proteins capable of either capping a microfilament when present as a nonphosphorylated monomer or stabilizing and protecting the microfilament when organized in small, phosphorylated oligomers.

摘要

肌动蛋白和小热休克蛋白(sHsps)是普遍存在且具有多方面功能的蛋白质,以两种可逆形式存在,即单体和多聚体,也就是细胞骨架的微丝和sHsps的寡聚体,通常认为呈球形中空形式。文献中描述了两种情况,其中sHsps可调节肌动蛋白的特性;在体外,一些sHsps作为封端蛋白可抑制肌动蛋白聚合,并且一些sHsps可保护肌动蛋白细胞骨架免受各种应激条件诱导的破坏。我们提出,肌动蛋白与sHsps之间存在直接相互作用,以抑制肌动蛋白聚合并参与肌动蛋白丝动力学的体内调节。肌动蛋白细胞骨架的保护作用将源于F-肌动蛋白与sHsps的相互作用,其中微丝将被磷酸化sHsps的小寡聚体覆盖。这两种蛋白质具有共同的结构基序,提示存在直接结合位点,但仍有待证实。一些sHsps与肌动蛋白细胞骨架相互作用时,作为肌动蛋白结合蛋白,当以非磷酸化单体形式存在时能够封端微丝,而当以小的磷酸化寡聚体形式存在时能够稳定和保护微丝。

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