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两类Arp2/3复合物小分子抑制剂的表征

Characterization of two classes of small molecule inhibitors of Arp2/3 complex.

作者信息

Nolen B J, Tomasevic N, Russell A, Pierce D W, Jia Z, McCormick C D, Hartman J, Sakowicz R, Pollard T D

机构信息

Department of Molecular Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA.

出版信息

Nature. 2009 Aug 20;460(7258):1031-4. doi: 10.1038/nature08231. Epub 2009 Aug 2.

Abstract

Polymerization of actin filaments directed by the actin-related protein (Arp)2/3 complex supports many types of cellular movements. However, questions remain regarding the relative contributions of Arp2/3 complex versus other mechanisms of actin filament nucleation to processes such as path finding by neuronal growth cones; this is because of the lack of simple methods to inhibit Arp2/3 complex reversibly in living cells. Here we describe two classes of small molecules that bind to different sites on the Arp2/3 complex and inhibit its ability to nucleate actin filaments. CK-0944636 binds between Arp2 and Arp3, where it appears to block movement of Arp2 and Arp3 into their active conformation. CK-0993548 inserts into the hydrophobic core of Arp3 and alters its conformation. Both classes of compounds inhibit formation of actin filament comet tails by Listeria and podosomes by monocytes. Two inhibitors with different mechanisms of action provide a powerful approach for studying the Arp2/3 complex in living cells.

摘要

由肌动蛋白相关蛋白(Arp)2/3复合物引导的肌动蛋白丝聚合作用支持多种类型的细胞运动。然而,关于Arp2/3复合物与肌动蛋白丝成核的其他机制在诸如神经元生长锥寻路等过程中的相对贡献仍存在疑问;这是因为缺乏在活细胞中可逆抑制Arp2/3复合物的简单方法。在此,我们描述了两类小分子,它们结合到Arp2/3复合物上的不同位点并抑制其使肌动蛋白丝成核的能力。CK - 0944636结合在Arp2和Arp3之间,在那里它似乎会阻止Arp2和Arp3转变为其活性构象。CK - 0993548插入到Arp3的疏水核心并改变其构象。这两类化合物都能抑制李斯特菌形成肌动蛋白丝彗尾以及单核细胞形成小体。两种具有不同作用机制的抑制剂为在活细胞中研究Arp2/3复合物提供了一种有力的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cc6/2780427/67dcdf3e111b/nihms125603f1.jpg

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