Department of Physics, University of Massachusetts Amherst, Amherst, MA 01003, USA.
J Phys Condens Matter. 2011 Sep 21;23(37):374104. doi: 10.1088/0953-8984/23/37/374104. Epub 2011 Aug 23.
The microtubule cytoskeleton, including the associated proteins, forms a complex network essential to multiple cellular processes. Microtubule-associated motor proteins, such as kinesin-1, travel on microtubules to transport membrane bound vesicles across the crowded cell. Other motors, such as cytoplasmic dynein and kinesin-5, are used to organize the cytoskeleton during mitosis. In order to understand the self-organization processes of motors on microtubules, we performed filament-gliding assays with kinesin-1 motors bound to the cover glass with a high density of microtubules on the surface. To observe microtubule organization, 3% of the microtubules were fluorescently labeled to serve as tracers. We find that microtubules in these assays are not confined to two dimensions and can cross one other. This causes microtubules to align locally with a relatively short correlation length. At high density, this local alignment is enough to create 'intersections' of perpendicularly oriented groups of microtubules. These intersections create vortices that cause microtubules to form loops. We characterize the radius of curvature and time duration of the loops. These different behaviors give insight into how crowded conditions, such as those in the cell, might affect motor behavior and cytoskeleton organization.
微管细胞骨架,包括相关蛋白,形成了一个复杂的网络,对多种细胞过程至关重要。微管相关的马达蛋白,如驱动蛋白-1,在微管上移动,将膜结合囊泡运输穿过拥挤的细胞。其他马达蛋白,如细胞质动力蛋白和驱动蛋白-5,用于在有丝分裂期间组织细胞骨架。为了了解马达蛋白在微管上的自组织过程,我们使用与表面高密度微管结合的驱动蛋白-1 马达进行了细丝滑动实验。为了观察微管组织,3%的微管被荧光标记作为示踪剂。我们发现,这些实验中的微管不限于二维,可以相互交叉。这导致微管在局部与相对较短的相关长度对齐。在高密度下,这种局部对齐足以创建垂直排列的微管组的“交点”。这些交点形成涡流,导致微管形成环。我们描述了环的曲率半径和持续时间。这些不同的行为揭示了拥挤的条件(如细胞内的条件)如何可能影响马达行为和细胞骨架组织。