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Nanoscale stiffness topography reveals structure and mechanics of the transport barrier in intact nuclear pore complexes

机译:纳米级刚度拓扑结构揭示了完整核孔复合物中传输屏障的结构和力学

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摘要

The nuclear pore complex (NPC) is the gate for transport between the cell nucleus and the cytoplasm. Small molecules cross the NPC by passive diffusion, but molecules larger than ∼5 nm must bind to nuclear transport receptors to overcome a selective barrier within the NPC1. Although the structure and shape of the cytoplasmic ring of the NPC are relatively well characterized2, 3, 4, 5, the selective barrier is situated deep within the central channel of the NPC and depends critically on unstructured nuclear pore proteins5, 6, and is therefore not well understood. Here, we show that stiffness topography7 with sharp atomic force microscopy tips can generate nanoscale cross-sections of the NPC. The cross-sections reveal two distinct structures, a cytoplasmic ring and a central plug structure, which are consistent with the three-dimensional NPC structure derived from electron microscopy2, 3, 4, 5. The central plug persists after reactivation of the transport cycle and resultant cargo release, indicating that the plug is an intrinsic part of the NPC barrier. Added nuclear transport receptors accumulate on the intact transport barrier and lead to a homogenization of the barrier stiffness. The observed nanomechanical properties in the NPC indicate the presence of a cohesive barrier to transport and are quantitatively consistent with the presence of a central condensate of nuclear pore proteins in the NPC channel.
机译:核孔复合物(NPC)是细胞核与细胞质之间运输的大门。小分子通过被动扩散穿过NPC,但是大于5 nm的分子必须与核转运受体结合才能克服NPC1中的选择性屏障。尽管NPC胞质环的结构和形状具有相对较好的特征2、3、4、5,但选择性屏障位于NPC中央通道的深处,并严重依赖于非结构化的核孔蛋白5、6,因此不太了解。在这里,我们显示具有尖锐原子力显微镜尖端的刚度形貌7可以产生NPC的纳米级截面。横截面显示了两个不同的结构,一个胞质环和一个中央栓塞结构,与从电子显微镜获得的三维NPC结构一致2、3、4、5。中央栓塞在重新激活运输周期后仍然存在。结果货物释放,表明堵塞物是NPC屏障的固有部分。添加的核转运受体积聚在完整的转运屏障上,并导致屏障刚度的均质化。在NPC中观察到的纳米力学性质表明存在运输的内聚屏障,并且在数量上与NPC通道中核孔蛋白的中央冷凝物一致。

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