Oda Toshiyuki, Abe Tatsuki, Yanagisawa Haruaki, Kikkawa Masahide
Department of Cell Biology and Anatomy, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan Department of Anatomy and Structural Biology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokatoh, Chuo, Yamanashi 409-3898, Japan
Department of Cell Biology and Anatomy, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
J Cell Sci. 2016 Apr 15;129(8):1547-51. doi: 10.1242/jcs.184598. Epub 2016 Mar 1.
The docking complex is a molecular complex necessary for assembly of outer dynein arms (ODAs) on the axonemal doublet microtubules (DMTs) in cilia and flagella. The docking complex is hypothesized to be a 24-nm molecular ruler because ODAs align along the DMTs with 24-nm periodicity. In this study, we rigorously tested this hypothesis using structural and genetic methods. We found that the ODAs can bind to DMTs and porcine microtubules with 24-nm periodicities even in the absence of the docking complexin vitro Using cryo-electron tomography and structural labeling, we observed that the docking complex took an unexpectedly flexible conformation and did not lie along the length of DMTs. In the absence of docking complex, ODAs were released from the DMT at relatively low ionic strength conditions, suggesting that the docking complex strengthens the electrostatic interactions between the ODA and DMT. Based on these results, we conclude that the docking complex serves as a flexible stabilizer of the ODA rather than as a molecular ruler.
对接复合体是在纤毛和鞭毛的轴丝双联微管(DMT)上组装外动力蛋白臂(ODA)所必需的分子复合体。对接复合体被假定为一个24纳米的分子尺,因为ODA沿着DMT以24纳米的周期排列。在本研究中,我们使用结构和遗传方法严格检验了这一假设。我们发现,即使在体外没有对接复合体的情况下,ODA也能以24纳米的周期与DMT和猪微管结合。使用冷冻电子断层扫描和结构标记,我们观察到对接复合体呈现出意想不到的灵活构象,并且并不沿着DMT的长度方向排列。在没有对接复合体的情况下,ODA在相对低离子强度条件下从DMT上释放,这表明对接复合体增强了ODA与DMT之间的静电相互作用。基于这些结果,我们得出结论,对接复合体作为ODA的一个灵活稳定剂,而非分子尺。