Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Annu Rev Biochem. 2011;80:613-43. doi: 10.1146/annurev-biochem-060109-151030.
In eukaryotic cells, the spatial segregation of replication and transcription in the nucleus and translation in the cytoplasm imposes the requirement of transporting thousands of macromolecules between these two compartments. Nuclear pore complexes (NPCs) are the sole gateways that facilitate this macromolecular exchange across the nuclear envelope with the help of soluble transport receptors. Whereas the mobile transport machinery is reasonably well understood at the atomic level, a commensurate structural characterization of the NPC has only begun in the past few years. Here, we describe the recent progress toward the elucidation of the atomic structure of the NPC, highlight emerging concepts of its underlying architecture, and discuss key outstanding questions and challenges. The applied structure determination as well as the described design principles of the NPC may serve as paradigms for other macromolecular assemblies.
在真核细胞中,细胞核内的复制和转录以及细胞质中的翻译在空间上是分隔开的,这就要求在这两个隔室之间运输数千种大分子。核孔复合物(NPC)是唯一的通道,它在可溶性转运受体的帮助下促进核膜上的这种大分子交换。虽然移动的转运机制在原子水平上已经得到了很好的理解,但 NPC 的结构特征在过去几年才刚刚开始。在这里,我们描述了阐明 NPC 原子结构的最新进展,强调了其基本结构的新出现的概念,并讨论了关键的悬而未决的问题和挑战。NPC 的应用结构测定以及所描述的设计原则可以作为其他大分子组装体的范例。