Yasuda R, Miyata H, Kinosita K
Department of Physics, Faculty of Science and Technology, Keio University Hiyoshi, Yokohama, Japan.
J Mol Biol. 1996 Oct 25;263(2):227-36. doi: 10.1006/jmbi.1996.0571.
Flexural and torsional rigidities of actin filaments are important factors in cell motility and muscle contraction, where actin filaments serve as mechanical elements. The flexural rigidity has already been determined by directly observing the bending of individual filaments under a microscope, but measurement of the torsional rigidity has been relatively scarce and indirect, because torsion of an actin filament is difficult to visualize. This paper shows that the torsional rigidity can be measured directly by visualizing the torsional Brownian motion of a single actin filament with a novel methodology based on an optical trapping technique. Actin filaments (F-actin) were prepared by polymerizing actin monomers binding Ca2+ ion or Mg2+ ion at the high affinity site. The torsional rigidity of F-Ca(2+)-actin ((8.5(+/- 1.3)) x 10(-26) N m2) was about three times as large as that of F-Mg(2+)-actin ((2.8(+/- 0.3)) x 10(-26) N m2), whereas the flexural rigidity ((6.0(+/- 0.2)) x 10(-26) N m2) was almost independent of the kind of the bound cation. The dynamic structure of F-actin is regulated by the bound metal in an anisotropic manner. The torsional rigidities above, whether of F-Ca(2+)-actin or F-Mg(2+)-actin, are one to two orders of magnitude greater than previous experimental estimates.
肌动蛋白丝的弯曲和扭转刚度是细胞运动和肌肉收缩中的重要因素,在这些过程中肌动蛋白丝充当机械元件。弯曲刚度已经通过在显微镜下直接观察单个丝的弯曲来确定,但扭转刚度的测量相对较少且间接,因为肌动蛋白丝的扭转很难可视化。本文表明,通过基于光镊技术的新方法可视化单个肌动蛋白丝的扭转布朗运动,可以直接测量扭转刚度。肌动蛋白丝(F-肌动蛋白)是通过在高亲和力位点聚合结合Ca2+离子或Mg2+离子的肌动蛋白单体来制备的。F-Ca(2+)-肌动蛋白的扭转刚度((8.5(±1.3))×10(-26) N m2)约为F-Mg(2+)-肌动蛋白((2.8(±0.3))×10(-26) N m2)的三倍,而弯曲刚度((6.0(±0.2))×10(-26) N m2)几乎与结合阳离子的种类无关。F-肌动蛋白的动态结构以各向异性方式由结合的金属调节。上述F-Ca(2+)-肌动蛋白或F-Mg(2+)-肌动蛋白的扭转刚度比先前的实验估计值大一个到两个数量级。