Department of Biology, Cell Biology, Neurobiology and Biophysics, Faculty of Science, Utrecht University , Utrecht, Netherlands.
J Cell Biol. 2023 May 1;222(5). doi: 10.1083/jcb.202106105. Epub 2023 Mar 2.
The microtubule (MT) cytoskeleton underlies processes such as intracellular transport and cell division. Immunolabeling for posttranslational modifications of tubulin has revealed the presence of different MT subsets, which are believed to differ in stability and function. Whereas dynamic MTs can readily be studied using live-cell plus-end markers, the dynamics of stable MTs have remained obscure due to a lack of tools to directly visualize these MTs in living cells. Here, we present StableMARK (Stable Microtubule-Associated Rigor-Kinesin), a live-cell marker to visualize stable MTs with high spatiotemporal resolution. We demonstrate that a rigor mutant of Kinesin-1 selectively binds to stable MTs without affecting MT organization and organelle transport. These MTs are long-lived, undergo continuous remodeling, and often do not depolymerize upon laser-based severing. Using this marker, we could visualize the spatiotemporal regulation of MT stability before, during, and after cell division. Thus, this live-cell marker enables the exploration of different MT subsets and how they contribute to cellular organization and transport.
微管(MT)细胞骨架支持细胞内运输和细胞分裂等过程。针对微管蛋白翻译后修饰的免疫标记揭示了不同的 MT 亚群的存在,这些亚群被认为在稳定性和功能上存在差异。虽然使用活细胞加尾标记可以很容易地研究动态 MT,但由于缺乏直接在活细胞中可视化这些 MT 的工具,稳定 MT 的动力学仍然不清楚。在这里,我们提出了 StableMARK(稳定微管相关刚性驱动蛋白),这是一种活细胞标记物,可高时空分辨率可视化稳定的 MT。我们证明,驱动蛋白-1 的刚性突变体选择性地与稳定的 MT 结合,而不影响 MT 组织和细胞器运输。这些 MT 寿命长,不断进行重塑,并且通常不会在基于激光的切割时解聚。使用这种标记物,我们可以在细胞分裂前后观察 MT 稳定性的时空调节。因此,这种活细胞标记物能够探索不同的 MT 亚群以及它们如何有助于细胞组织和运输。