Oda Toshiro, Iwasa Mitsusada, Aihara Tomoki, Maéda Yuichiro, Narita Akihiro
X-ray Structural Analysis Research Team, RIKEN SPring-8 Center, RIKEN Harima Institute, 1-1-1, Kouto, Sayo, Hyogo 679-5148, Japan.
Nature. 2009 Jan 22;457(7228):441-5. doi: 10.1038/nature07685.
Actin plays crucial parts in cell motility through a dynamic process driven by polymerization and depolymerization, that is, the globular (G) to fibrous (F) actin transition. Although our knowledge about the actin-based cellular functions and the molecules that regulate the G- to F-actin transition is growing, the structural aspects of the transition remain enigmatic. We created a model of F-actin using X-ray fibre diffraction intensities obtained from well oriented sols of rabbit skeletal muscle F-actin to 3.3 A in the radial direction and 5.6 A along the equator. Here we show that the G- to F-actin conformational transition is a simple relative rotation of the two major domains by about 20 degrees. As a result of the domain rotation, the actin molecule in the filament is flat. The flat form is essential for the formation of stable, helical F-actin. Our F-actin structure model provides the basis for understanding actin polymerization as well as its molecular interactions with actin-binding proteins.
肌动蛋白通过由聚合和解聚驱动的动态过程,即在球状(G)肌动蛋白向纤维状(F)肌动蛋白的转变过程中,在细胞运动中发挥关键作用。尽管我们对基于肌动蛋白的细胞功能以及调节G向F肌动蛋白转变的分子的了解不断增加,但转变的结构方面仍然神秘莫测。我们利用从兔骨骼肌F肌动蛋白的良好定向溶胶中获得的X射线纤维衍射强度,创建了一个F肌动蛋白模型,该模型在径向方向上分辨率达到3.3 Å,在赤道方向上分辨率达到5.6 Å。在这里,我们表明G向F肌动蛋白的构象转变是两个主要结构域大约20度的简单相对旋转。由于结构域的旋转,细丝中的肌动蛋白分子是扁平的。这种扁平形式对于形成稳定的螺旋状F肌动蛋白至关重要。我们的F肌动蛋白结构模型为理解肌动蛋白聚合及其与肌动蛋白结合蛋白的分子相互作用提供了基础。