Schroer T A, Schnapp B J, Reese T S, Sheetz M P
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110.
J Cell Biol. 1988 Nov;107(5):1785-92. doi: 10.1083/jcb.107.5.1785.
Kinesin is a force-generating ATPase that drives the sliding movement of microtubules on glass coverslips and the movement of plastic beads along microtubules. Although kinesin is suspected to participate in microtubule-based organelle transport, the exact role it plays in this process is unclear. To address this question, we have developed a quantitative assay that allows us to determine the ability of soluble factors to promote organelle movement. Salt-washed organelles from squid axoplasm exhibited a nearly undetectable level of movement on purified microtubules. Their frequency of movement could be increased greater than 20-fold by the addition of a high speed axoplasmic supernatant. Immunoadsorption of kinesin from this supernatant decreased the frequency of organelle movement by more than 70%; organelle movements in both directions were markedly reduced. Surprisingly, antibody purified kinesin did not promote organelle movement either by itself or when it was added back to the kinesin-depleted supernatant. This result suggested that other soluble factors necessary for organelle movement were removed along with kinesin during immunoadsorption of the supernatant. A high level of organelle motor activity was recovered in a high salt eluate of the immunoadsorbent that contained only little kinesin. On the basis of these results we propose that organelle movement on microtubules involves other soluble axoplasmic factors in addition to kinesin.
驱动蛋白是一种能产生力的ATP酶,它能推动微管在玻璃盖玻片上滑动以及塑料珠沿着微管移动。尽管怀疑驱动蛋白参与基于微管的细胞器运输,但它在这一过程中的确切作用尚不清楚。为了解决这个问题,我们开发了一种定量分析方法,使我们能够确定可溶性因子促进细胞器移动的能力。从鱿鱼轴质中经盐洗的细胞器在纯化的微管上显示出几乎检测不到的移动水平。通过添加高速轴质上清液,它们的移动频率可提高20倍以上。从该上清液中免疫吸附驱动蛋白可使细胞器移动频率降低70%以上;双向的细胞器移动均明显减少。令人惊讶的是,抗体纯化的驱动蛋白无论是自身还是添加回耗尽驱动蛋白的上清液中,都不能促进细胞器移动。这一结果表明,在上清液的免疫吸附过程中,细胞器移动所需的其他可溶性因子与驱动蛋白一起被去除了。在仅含有少量驱动蛋白的免疫吸附剂的高盐洗脱液中恢复了高水平的细胞器运动活性。基于这些结果,我们提出微管上的细胞器移动除驱动蛋白外还涉及其他可溶性轴质因子。