Satir P, Sale W S
J Protozool. 1977 Nov;24(4):498-501. doi: 10.1111/j.1550-7408.1977.tb00999.x.
The source of force generation of beating cilia and flagella is an interaction between the doublet microtubules mediated by the dynein-1 arms which cause the doublets to slide relative to one another. Previously, were domonstrated direct sliding of Tetrahymena ciliary axonemes by dark field light microscopy. In this paper, the results of such an experiment have been captured on a polylysine-coated grid surface for whole-mount electron microscopy. Image in which a constant polarity. To produce the observed displacement, the direction of the dynein-1 arm force generation must be from base to tip, so that the doublet (n), to which the arms are attached, pushes the next doublet (n + 1) toward the tip. In addition to the functional polarity, the dynein-1 arms are found to have a structural polarity: they tilt toward the base when viewed along the edges of the A-subfiber. A scheme is presented which reconciles the finding of a single polarity of active sliding with the geometry of microtubule tip displacement of bent cilia.
纤毛和鞭毛摆动产生力的来源是由动力蛋白-1臂介导的双联微管之间的相互作用,这种相互作用导致双联微管相互相对滑动。此前,通过暗视野光学显微镜证实了四膜虫纤毛轴丝的直接滑动。在本文中,此类实验的结果已在用于整装电子显微镜观察的聚赖氨酸包被的网格表面上捕获。图像具有恒定的极性。为了产生观察到的位移,动力蛋白-1臂产生力的方向必须从基部指向尖端,这样,臂所附着的双联微管(n)就会将下一个双联微管(n + 1)推向尖端。除了功能极性外,还发现动力蛋白-1臂具有结构极性:当沿着A亚纤维的边缘观察时,它们向基部倾斜。本文提出了一个方案,该方案将主动滑动单一极性的发现与弯曲纤毛微管尖端位移的几何形状协调起来。