College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang 310024, China; Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou, Zhejiang 310024, China; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang 310024, China; Institute of Biology, Westlake Institute for Advanced Study, Hangzhou, Zhejiang 310024, China.
Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou, Zhejiang 310024, China; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang 310024, China; Institute of Biology, Westlake Institute for Advanced Study, Hangzhou, Zhejiang 310024, China.
Cell. 2024 Oct 3;187(20):5638-5650.e18. doi: 10.1016/j.cell.2024.08.002. Epub 2024 Aug 27.
The protein import motor in chloroplasts plays a pivotal role in their biogenesis and homeostasis by driving the translocation of preproteins into chloroplasts. While the Ycf2-FtsHi complex serves as the import motor in land plants, its evolutionary conservation, specialization, and mechanisms across photosynthetic organisms are largely unexplored. Here, we isolated and determined the cryogenic electron microscopy (cryo-EM) structures of the native Ycf2-FtsHi complex from Chlamydomonas reinhardtii, uncovering a complex composed of up to 19 subunits, including multiple green-algae-specific components. The heterohexameric AAA+ ATPase motor module is tilted, potentially facilitating preprotein handover from the translocon at the inner chloroplast membrane (TIC) complex. Preprotein interacts with Ycf2-FtsHi and enhances its ATPase activity in vitro. Integrating Ycf2-FtsHi and translocon at the outer chloroplast membrane (TOC)-TIC supercomplex structures reveals insights into their physical and functional interplay during preprotein translocation. By comparing these findings with those from land plants, our study establishes a structural foundation for understanding the assembly, function, evolutionary conservation, and diversity of chloroplast protein import motors.
叶绿体中的蛋白输入马达通过驱动前体蛋白进入叶绿体,在其生物发生和动态平衡中发挥关键作用。虽然 Ycf2-FtsHi 复合物作为陆地植物的输入马达,但它在光合生物中的进化保守性、专业化和机制在很大程度上仍未被探索。在这里,我们从莱茵衣藻中分离并确定了天然 Ycf2-FtsHi 复合物的低温电子显微镜 (cryo-EM) 结构,揭示了一个由多达 19 个亚基组成的复合物,包括多个绿藻特异性成分。异六聚体 AAA+ATP 酶马达模块倾斜,可能有助于将前体蛋白从内叶绿体膜 (TIC) 复合物上的转位器中传递出去。前体蛋白与 Ycf2-FtsHi 相互作用,并在体外增强其 ATP 酶活性。整合 Ycf2-FtsHi 和外叶绿体膜 (TOC)-TIC 超复合物结构揭示了它们在前体蛋白转运过程中物理和功能相互作用的见解。通过将这些发现与陆地植物进行比较,我们的研究为理解叶绿体蛋白输入马达的组装、功能、进化保守性和多样性奠定了结构基础。