核孔
核孔蛋白
低温电子显微
结构生物学
电子显微镜
分辨率(逻辑)
显微镜
低温电子层析成像
电子晶体学
化学
结晶学
生物物理学
纳米技术
材料科学
生物
物理
核运输
电子衍射
细胞核
细胞质
衍射
计算机科学
生物化学
光学
人工智能
断层摄影术
作者
Linhua Tai,Guoliang Yin,Fei Sun,Yun Zhu
标识
DOI:10.1016/j.jmb.2023.168051
摘要
The nuclear pore complex (NPC) is a giant protein assembly that penetrates the double layers of the nuclear membrane. The overall structure of the NPC has approximately eightfold symmetry and is formed by approximately 30 nucleoporins. The great size and complexity of the NPC have hindered the study of its structure for many years until recent breakthroughs were achieved by integrating the latest high-resolution cryo-electron microscopy (cryo-EM), the emerging artificial intelligence-based modeling and all other available structural information from crystallography and mass spectrometry. Here, we review our latest knowledge of the NPC architecture and the history of its structural study from in vitro to in situ with progressively improved resolutions by cryo-EM, with a particular focus on the latest subnanometer-resolution structural studies. The future directions for structural studies of NPCs are also discussed.
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