Toba Shiori, Watanabe Tomonobu M, Yamaguchi-Okimoto Lisa, Toyoshima Yoko Yano, Higuchi Hideo
Department of Life Sciences, Graduate School of Arts and Sciences, University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan.
Proc Natl Acad Sci U S A. 2006 Apr 11;103(15):5741-5. doi: 10.1073/pnas.0508511103. Epub 2006 Apr 3.
Structural differences between dynein and kinesin suggest a unique molecular mechanism of dynein motility. Measuring the mechanical properties of a single molecule of dynein is crucial for revealing the mechanisms underlying its movement. We measured the step size and force produced by single molecules of active cytoplasmic dynein by using an optical trap and fluorescence imaging with a high temporal resolution. The velocity of dynein movement, 800 nm/s, is consistent with that reported in cells. The maximum force of 7-8 pN was independent of the ATP concentration and similar to that of kinesin. Dynein exhibited forward and occasional backwards steps of approximately 8 nm, independent of load. It is suggested that the large dynein heads take 16-nm steps by using an overlapping hand-over-hand mechanism.
动力蛋白和驱动蛋白之间的结构差异表明了动力蛋白运动的独特分子机制。测量单个动力蛋白分子的力学性质对于揭示其运动背后的机制至关重要。我们通过使用光镊和具有高时间分辨率的荧光成像来测量活性细胞质动力蛋白单个分子产生的步长和力。动力蛋白的运动速度为800nm/s,与细胞中报道的速度一致。7-8 pN的最大力与ATP浓度无关,且与驱动蛋白的最大力相似。动力蛋白表现出大约8nm的向前和偶尔向后的步长,与负载无关。有人提出,大型动力蛋白头部通过使用重叠的手拉手机制采取16nm的步长。