Bioactive Functionalized Monolayer Graphene for High-Resolution Cryo-Electron Microscopy

被引:70
作者
Liu, Nan [1 ,2 ]
Zhang, Jincan [3 ,4 ]
Chen, Yanan [1 ]
Liu, Chuan [1 ]
Zhang, Xing [1 ]
Xu, Kui [1 ,2 ]
Wen, Jie [1 ]
Luo, Zhipu [1 ]
Chen, Shulin [5 ,6 ]
Gao, Peng [5 ,6 ,7 ]
Jia, Kaicheng [3 ]
Liu, Zhongfan [3 ]
Peng, Hailin [3 ,4 ]
Wang, Hong-Wei [1 ,2 ]
机构
[1] Tsinghua Univ, Sch Life Sci, Beijing Adv Innovat Ctr Struct Biol, Minist Educ,Key Lab Prot Sci, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Tsinghua Peking Joint Ctr Life Sci, Beijing 100084, Peoples R China
[3] Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, Ctr Nanochem,Beijing Sci & Engn Ctr Nanocarbons, Beijing 100871, Peoples R China
[4] Peking Univ, Sch Phys, Acad Adv Interdisciplinary Studies, Beijing 100871, Peoples R China
[5] Peking Univ, Sch Phys, Int Ctr Quantum Mat, Beijing 100871, Peoples R China
[6] Peking Univ, Sch Phys, Electron Microscopy Lab, Beijing 100871, Peoples R China
[7] Collaborat Innovat Ctr Quantum Matter, Beijing 100871, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
BEAM-INDUCED MOTION; CRYO-EM; MACROMOLECULAR COMPLEXES; ELECTRON-MICROSCOPY; 20S PROTEASOME; OXIDE; CONDUCTIVITY; FILMS; VITRIFICATION; VISUALIZATION;
D O I
10.1021/jacs.8b13038
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-particle cryo-electron microscopy (cryo-EM) has become one of the most essential tools to understand biological mechanisms at molecular level. A major bottleneck in cryo-EM technique is the preparation of good specimens that embed biological macromolecules in a thin layer of vitreous ice. In the canonical cryo-EM specimen preparation method, biological macromolecules tend to be adsorbed to the air-water interface, causing partial denaturation and/or preferential orientations. In this work, we have designed and produced a new type of cryo-EM grids using bioactive-ligand functionalized single-crystalline monolayer graphene membranes as supporting films. The functionalized graphene membrane (FGM) grids exhibit specific binding affinity to histidine (His)-tagged proteins and complexes. In cryo-EM, the FGM grids generate relatively low background for imaging and selectively anchor 20S proteasomes to the supporting film surface, enabling near- atomic-resolution 3D reconstruction of the complex. We envision that the FGM grids could benefit single particle cryo-EM specimen preparation with high reproducibility and robustness, therefore enhancing the efficiency and throughput of high-resolution cryo-EM structural determination.
引用
收藏
页码:4016 / 4025
页数:10
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