Mitra Aniruddha, Loseva Elizaveta, Peterman Erwin J G
Department of Physics and Astronomy and LaserLaB, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands.
Nat Commun. 2024 Apr 24;15(1):3456. doi: 10.1038/s41467-024-47807-2.
Intraflagellar transport (IFT) orchestrates entry of proteins into primary cilia. At the ciliary base, assembled IFT trains, driven by kinesin-2 motors, can transport cargo proteins into the cilium, across the crowded transition zone. How trains assemble at the base and how proteins associate with them is far from understood. Here, we use single-molecule imaging in the cilia of C. elegans chemosensory neurons to directly visualize the entry of kinesin-2 motors, kinesin-II and OSM-3, as well as anterograde cargo proteins, IFT dynein and tubulin. Single-particle tracking shows that IFT components associate with trains sequentially, both in time and space. Super-resolution maps of IFT components in wild-type and mutant worms reveal ciliary ultrastructure and show that kinesin-II is essential for axonemal organization. Finally, imaging cilia lacking kinesin-II and/or transition zone function uncovers the interplay of kinesin-II and OSM-3 in driving efficient transport of IFT trains across the transition zone.
鞭毛内运输(IFT)协调蛋白质进入初级纤毛的过程。在纤毛基部,由驱动蛋白-2马达驱动的组装好的IFT列车能够将货物蛋白运输到纤毛中,穿过拥挤的过渡区。列车如何在基部组装以及蛋白质如何与它们结合仍远未可知。在这里,我们利用秀丽隐杆线虫化学感受神经元纤毛中的单分子成像技术,直接观察驱动蛋白-2马达、驱动蛋白-II和OSM-3以及顺行货物蛋白、IFT动力蛋白和微管蛋白的进入情况。单粒子追踪显示,IFT组件在时间和空间上依次与列车结合。野生型和突变型蠕虫中IFT组件的超分辨率图谱揭示了纤毛超微结构,并表明驱动蛋白-II对轴丝组织至关重要。最后,对缺乏驱动蛋白-II和/或过渡区功能的纤毛进行成像,揭示了驱动蛋白-II和OSM-3在驱动IFT列车有效穿过过渡区中的相互作用。