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

TitleBioactive Functionalized Monolayer Graphene for High-Resolution Cryo-Electron Microscopy
Authors
Issue Date2019
Citation
Journal of the American Chemical Society, 2019, v. 141, n. 9, p. 4016-4025 How to Cite?
AbstractSingle-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.
Persistent Identifierhttp://hdl.handle.net/10722/351388
ISSN
2023 Impact Factor: 14.4
2023 SCImago Journal Rankings: 5.489

 

DC FieldValueLanguage
dc.contributor.authorLiu, Nan-
dc.contributor.authorZhang, Jincan-
dc.contributor.authorChen, Yanan-
dc.contributor.authorLiu, Chuan-
dc.contributor.authorZhang, Xing-
dc.contributor.authorXu, Kui-
dc.contributor.authorWen, Jie-
dc.contributor.authorLuo, Zhipu-
dc.contributor.authorChen, Shulin-
dc.contributor.authorGao, Peng-
dc.contributor.authorJia, Kaicheng-
dc.contributor.authorLiu, Zhongfan-
dc.contributor.authorPeng, Hailin-
dc.contributor.authorWang, Hong Wei-
dc.date.accessioned2024-11-20T03:55:59Z-
dc.date.available2024-11-20T03:55:59Z-
dc.date.issued2019-
dc.identifier.citationJournal of the American Chemical Society, 2019, v. 141, n. 9, p. 4016-4025-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10722/351388-
dc.description.abstractSingle-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.-
dc.languageeng-
dc.relation.ispartofJournal of the American Chemical Society-
dc.titleBioactive Functionalized Monolayer Graphene for High-Resolution Cryo-Electron Microscopy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/jacs.8b13038-
dc.identifier.pmid30724081-
dc.identifier.scopuseid_2-s2.0-85062353026-
dc.identifier.volume141-
dc.identifier.issue9-
dc.identifier.spage4016-
dc.identifier.epage4025-
dc.identifier.eissn1520-5126-

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