Department of Molecular and Cellular Medicine, Texas A&M University, College of Medicine, The Texas A&M Health Science Center, College Station, TX, USA.
Nat Cell Biol. 2022 Jan;24(1):112-122. doi: 10.1038/s41556-021-00815-6. Epub 2022 Jan 10.
Nuclear pore complexes (NPCs) embedded within the nuclear envelope mediate rapid, selective and bidirectional traffic between the cytoplasm and the nucleoplasm. Deciphering the mechanism and dynamics of this process is challenged by the need for high spatial and temporal resolution. We report here a multicolour imaging approach that enables direct three-dimensional visualization of cargo transport trajectories relative to a super-resolved octagonal double-ring structure of the NPC scaffold. The success of this approach is enabled by the high positional stability of NPCs within permeabilized cells, as verified by a combined experimental and simulation analysis. Hourglass-shaped translocation conduits for two cargo complexes representing different nuclear transport receptor pathways indicate rapid migration through the permeability barrier on or near the NPC scaffold. Binding sites for cargo complexes extend more than 100 nm from the pore openings, which is consistent with a wide distribution of the phenylalanine-glycine polypeptides that bind nuclear transport receptors.
核孔复合体(NPC)嵌入核膜中,介导细胞质和核质之间快速、选择性和双向的物质运输。由于需要高时空分辨率,因此解析这个过程的机制和动力学具有挑战性。我们在这里报告了一种多色成像方法,能够直接三维可视化相对于 NPC 支架的超分辨八重双环结构的货物运输轨迹。这种方法的成功得益于在通透细胞中 NPC 具有高的位置稳定性,这通过组合实验和模拟分析得到了验证。代表不同核转运受体途径的两个货物复合物的沙漏形易位导管所指示的是在 NPC 支架上或附近快速通过通透性屏障的迁移。货物复合物的结合位点从孔开口延伸超过 100nm,这与结合核转运受体的苯丙氨酸-甘氨酸多肽的广泛分布一致。