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调节Arp2/3介导的肌动蛋白组装的蛋白质复合物。

Protein complexes regulating Arp2/3-mediated actin assembly.

作者信息

Stradal Theresia E B, Scita Giorgio

机构信息

Signalling and Motility Group, German Research Centre for Biotechnology (GBF), Mascheroder Weg 1, D-38124 Braunschweig, Germany.

出版信息

Curr Opin Cell Biol. 2006 Feb;18(1):4-10. doi: 10.1016/j.ceb.2005.12.003. Epub 2005 Dec 15.

Abstract

Key steps in regulating actin dynamics are the de novo nucleation and elongation of actin filaments, which can be catalysed by a limited number of proteins and protein complexes. Among these, Arp2/3 complex and formins are the best studied. Arp2/3-complex activity is controlled through signalling-dependent association with nucleation-promoting factors, such as the WASP/WAVE family proteins. A common theme for these molecules, which is well established for WAVEs but is only just beginning to emerge for WASPs, is that they act as coincident detectors of a variety of signalling pathways through the formation of large multi-molecular complexes.

摘要

调节肌动蛋白动力学的关键步骤是肌动蛋白丝的从头成核和延伸,这可由有限数量的蛋白质和蛋白质复合物催化。其中,Arp2/3复合物和formin是研究得最为深入的。Arp2/3复合物的活性通过与成核促进因子(如WASP/WAVE家族蛋白)的信号依赖性结合来控制。这些分子的一个共同特点,在WAVE中已得到充分证实,但在WASP中才刚刚开始显现,即它们通过形成大型多分子复合物,作为多种信号通路的同步检测器。

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