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肌动蛋白丝帽蛋白 Twinfilin 对肌动蛋白丝的封端作用的结构基础及进化起源

Structural basis and evolutionary origin of actin filament capping by twinfilin.

作者信息

Paavilainen Ville O, Hellman Maarit, Helfer Emmanuèle, Bovellan Miia, Annila Arto, Carlier Marie-France, Permi Perttu, Lappalainen Pekka

机构信息

Program in Cellular Biotechnology and Structural Biology and Biophysics, Institute of Biotechnology, University of Helsinki, FI-00014, Finland.

出版信息

Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3113-8. doi: 10.1073/pnas.0608725104. Epub 2007 Feb 20.

Abstract

Dynamic reorganization of the actin cytoskeleton is essential for motile and morphological processes in all eukaryotic cells. One highly conserved protein that regulates actin dynamics is twinfilin, which both sequesters actin monomers and caps actin filament barbed ends. Twinfilin is composed of two ADF/cofilin-like domains, Twf-N and Twf-C. Here, we reveal by systematic domain-swapping/inactivation analysis that the two functional ADF-H domains of twinfilin are required for barbed-end capping and that Twf-C plays a critical role in this process. However, these domains are not functionally equivalent. NMR-structure and mutagenesis analyses, together with biochemical and motility assays showed that Twf-C, in addition to its binding to G-actin, interacts with the sides of actin filaments like ADF/cofilins, whereas Twf-N binds only G-actin. Our results indicate that during filament barbed-end capping, Twf-N interacts with the terminal actin subunit, whereas Twf-C binds between two adjacent subunits at the side of the filament. Thus, the domain requirement for actin filament capping by twinfilin is remarkably similar to that of gelsolin family proteins, suggesting the existence of a general barbed-end capping mechanism. Furthermore, we demonstrate that a synthetic protein consisting of duplicated ADF/cofilin domains caps actin filament barbed ends, providing evidence that the barbed-end capping activity of twinfilin arose through a duplication of an ancient ADF/cofilin-like domain.

摘要

肌动蛋白细胞骨架的动态重组对于所有真核细胞的运动和形态形成过程至关重要。一种高度保守的调节肌动蛋白动力学的蛋白质是双丝蛋白,它既能隔离肌动蛋白单体,又能封闭肌动蛋白丝的带刺末端。双丝蛋白由两个ADF/丝切蛋白样结构域Twf-N和Twf-C组成。在这里,我们通过系统的结构域交换/失活分析揭示,双丝蛋白的两个功能性ADF-H结构域是封闭带刺末端所必需的,并且Twf-C在这个过程中起关键作用。然而,这些结构域在功能上并不等同。核磁共振结构和诱变分析,以及生化和运动分析表明,Twf-C除了与G-肌动蛋白结合外,还像ADF/丝切蛋白一样与肌动蛋白丝的侧面相互作用,而Twf-N只与G-肌动蛋白结合。我们的结果表明,在细丝带刺末端封闭过程中,Twf-N与末端肌动蛋白亚基相互作用,而Twf-C在细丝侧面的两个相邻亚基之间结合。因此,双丝蛋白封闭肌动蛋白丝所需的结构域与凝溶胶蛋白家族蛋白非常相似,这表明存在一种普遍的带刺末端封闭机制。此外,我们证明由重复的ADF/丝切蛋白结构域组成的合成蛋白能够封闭肌动蛋白丝的带刺末端,这为双丝蛋白的带刺末端封闭活性是通过古老的ADF/丝切蛋白样结构域的复制产生的提供了证据。

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