Kotani Norito, Sakakibara Hitoshi, Burgess Stan A, Kojima Hiroaki, Oiwa Kazuhiro
Graduate School of Life Science, University of Hyogo, Harima Science Park City, Hyogo 6781297, Japan.
Biophys J. 2007 Aug 1;93(3):886-94. doi: 10.1529/biophysj.106.101964. Epub 2007 May 11.
Inner-arm dynein-f of Chlamydomonas flagella is a heterodimeric dynein. We performed conventional in vitro motility assays showing that dynein-f translocates microtubules at the comparatively low velocity of approximately 1.2 microm/s. From the dependence of velocity upon the surface density of dynein-f, we estimate its duty ratio to be 0.6-0.7. The relation between microtubule landing rate and surface density of dynein-f are well fitted by the first-power dependence, as expected for a processive motor. At low dynein densities, progressing microtubules rotate erratically about a fixed point on the surface, at which a single dynein-f molecule is presumably located. We conclude that dynein-f has high processivity. In an axoneme, however, slow and processive dynein-f could impede microtubule sliding driven by other fast dyneins (e.g., dynein-c). To obtain insight into the in vivo roles of dynein-f, we measured the sliding velocity of microtubules driven by a mixture of dyneins -c and -f at various mixing ratios. The velocity is modulated as a function of the ratio of dynein-f in the mixture. This modulation suggests that dynein-f acts as a load in the axoneme, but force pushing dynein-f molecules forward seems to accelerate their dissociation from microtubules.
衣藻鞭毛的内臂动力蛋白f是一种异源二聚体动力蛋白。我们进行了传统的体外运动分析,结果表明动力蛋白f以相对较低的速度(约1.2微米/秒)使微管移位。根据速度对动力蛋白f表面密度的依赖性,我们估计其工作比为0.6 - 0.7。微管着陆率与动力蛋白f表面密度之间的关系符合一次幂依赖性,这是持续性运动蛋白所预期的。在低动力蛋白密度下,前进的微管在表面的一个固定点周围不规则地旋转,推测该点有单个动力蛋白f分子。我们得出结论,动力蛋白f具有高持续性。然而,在轴丝中,缓慢且具持续性的动力蛋白f可能会阻碍由其他快速动力蛋白(如动力蛋白c)驱动的微管滑动。为了深入了解动力蛋白f在体内的作用,我们测量了由动力蛋白c和f的混合物以各种混合比例驱动时微管的滑动速度。速度随混合物中动力蛋白f的比例而调节。这种调节表明动力蛋白f在轴丝中起到负载的作用,但推动动力蛋白f分子向前的力似乎会加速它们从微管上解离。