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

机译:两类Arp2 / 3复合物的小分子抑制剂的表征

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摘要

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.
机译:由肌动蛋白相关蛋白(Arp)2/3复合体控制的肌动蛋白丝聚合可以支持许多类型的细胞运动。然而,关于Arp2 / 3复合物与肌动蛋白丝成核的其他机制相对于其他过程(例如通过神经元生长锥寻找路径)的相对贡献仍然存在疑问。这是因为缺乏在活细胞中可逆地抑制Arp2 / 3复合物的简单方法。在这里,我们描述了两类与Arp2 / 3复合物上不同位点结合并抑制其使肌动蛋白丝成核的能力的小分子。 CK-0944636在Arp2和Arp3之间绑定,似乎阻止了Arp2和Arp3进入其主动构象。 CK-0993548插入Arp3的疏水核中并改变其构象。这两类化合物均抑制李斯特菌引起的肌动蛋白丝彗星尾的形成,并抑制单核细胞形成的足囊。两种具有不同作用机理的抑制剂为研究活细胞中的Arp2 / 3复合物提供了有力的方法。

著录项

  • 来源
    《Nature》 |2009年第7258期|1031-1034|共4页
  • 作者单位

    Department of Molecular Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA Department of Cell Biology, Yale University, New Haven, Connecticut 06520, USA Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA Department of Chemistry and the Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403, USA;

    Cytokinetics, Inc., South San Francisco, California 94080, USA Kalobios Pharmaceuticals, Inc., South San Francisco, California 94080, USA;

    Cytokinetics, Inc., South San Francisco, California 94080, USA;

    Cytokinetics, Inc., South San Francisco, California 94080, USA Five Prime Therapeutics, San Francisco, California 94158, USA;

    Cytokinetics, Inc., South San Francisco, California 94080, USA;

    Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA;

    Cytokinetics, Inc., South San Francisco, California 94080, USA;

    Cytokinetics, Inc., South San Francisco, California 94080, USA Gilead Sciences, Inc., Foster City, California 94404, USA;

    Department of Molecular Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA Department of Cell Biology, Yale University, New Haven, Connecticut 06520, USA Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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