Volkmann Niels, Page Christopher, Li Rong, Hanein Dorit
Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Eur J Cell Biol. 2014 May-Jun;93(5-6):179-83. doi: 10.1016/j.ejcb.2014.01.003. Epub 2014 Jan 25.
The primary function of Arp2/3 complex is the generation of free barbed ends by nucleating new filaments from the sides of pre-existing filaments. The pathway of branch formation is complex and involves nucleation promoting factors, actin monomers and nucleotides. A less prominent function of Arp2/3 complex is capping of actin filament pointed ends. Here we show, using electron microscopy, electron tomography, and image reconstruction of negatively-stained samples at ∼2-3nm resolution, that Arp2/3 complex bound to the pointed ends of actin filaments has a conformation similar to that in the branch junction with the Arps arranged in an actin-filament like configuration. This is direct evidence for the existence of two distinct activation pathways for Arp2/3 complex, one in the context of branch formation, one in the context of pointed-end capping, with essentially the same conformational end point.
Arp2/3复合物的主要功能是通过在已有肌动蛋白丝的侧面成核新的肌动蛋白丝来产生游离的带刺末端。分支形成的途径很复杂,涉及成核促进因子、肌动蛋白单体和核苷酸。Arp2/3复合物一个不太显著的功能是封闭肌动蛋白丝的尖端。在这里,我们通过电子显微镜、电子断层扫描以及对负染样品进行约2 - 3纳米分辨率的图像重建显示,与肌动蛋白丝尖端结合的Arp2/3复合物具有与分支连接处相似的构象,其中Arp以类似肌动蛋白丝的构型排列。这是Arp2/3复合物存在两种不同激活途径的直接证据,一种是在分支形成的情况下,另一种是在尖端封闭的情况下,两者具有基本相同的构象终点。