Suppr超能文献

冷冻电子显微镜揭示核孔复合物的结构。

Cryo-electron Microscopy Reveals the Structure of the Nuclear Pore Complex.

机构信息

National Key Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address: https://twitter.com/TLinhua.

National Key Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

J Mol Biol. 2023 May 1;435(9):168051. doi: 10.1016/j.jmb.2023.168051. Epub 2023 Mar 17.

Abstract

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.

摘要

核孔复合体(NPC)是一种穿透核膜双层的巨大蛋白复合物。NPC 的整体结构具有大约 8 重对称性,由大约 30 个核孔蛋白组成。NPC 的巨大尺寸和复杂性多年来一直阻碍着其结构的研究,直到最近通过整合最新的高分辨率冷冻电镜(cryo-EM)、新兴的基于人工智能的建模以及来自晶体学和质谱的所有其他可用结构信息,才取得了突破。在这里,我们回顾了我们最新的 NPC 结构知识以及其结构研究的历史,从体外到原位,冷冻电镜的分辨率逐渐提高,特别关注最新的亚纳米分辨率结构研究。还讨论了 NPC 结构研究的未来方向。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验