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Dual-Affinity Graphene Sheets for High-Resolution Cryo-Electron Microscopy
[Image: see text] With the development of cryo-electron microscopy (cryo-EM), high-resolution structures of macromolecules can be reconstructed by the single particle method efficiently. However, challenges may still persist during the specimen preparation stage. Specifically, proteins tend to adsor...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103130/ https://www.ncbi.nlm.nih.gov/pubmed/37011903 http://dx.doi.org/10.1021/jacs.3c00659 |
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author | Cheng, Hang Zheng, Liming Liu, Nan Huang, Congyuan Xu, Jie Lu, Ye Cui, Xiaoya Xu, Kui Hou, Yuan Tang, Junchuan Zhang, Zhong Li, Jing Ni, Xiaodan Chen, Yanan Peng, Hailin Wang, Hong-Wei |
author_facet | Cheng, Hang Zheng, Liming Liu, Nan Huang, Congyuan Xu, Jie Lu, Ye Cui, Xiaoya Xu, Kui Hou, Yuan Tang, Junchuan Zhang, Zhong Li, Jing Ni, Xiaodan Chen, Yanan Peng, Hailin Wang, Hong-Wei |
author_sort | Cheng, Hang |
collection | PubMed |
description | [Image: see text] With the development of cryo-electron microscopy (cryo-EM), high-resolution structures of macromolecules can be reconstructed by the single particle method efficiently. However, challenges may still persist during the specimen preparation stage. Specifically, proteins tend to adsorb at the air–water interface and exhibit a preferred orientation in vitreous ice. To overcome these challenges, we have explored dual-affinity graphene (DAG) modified with two different affinity ligands as a supporting material for cryo-EM sample preparation. The ligands can bind to distinct sites on the corresponding tagged particles, which in turn generates various orientation distributions of particles and prevents the adsorption of protein particles onto the air–water interface. As expected, the DAG exhibited high binding specificity and affinity to target macromolecules, resulting in more balanced particle Euler angular distributions compared to single functionalized graphene on two different protein cases, including the SARS -CoV-2 spike glycoprotein. We anticipate that the DAG grids will enable facile and efficient three-dimensional (3D) reconstruction for cryo-EM structural determination, providing a robust and general technique for future studies. |
format | Online Article Text |
id | pubmed-10103130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101031302023-04-15 Dual-Affinity Graphene Sheets for High-Resolution Cryo-Electron Microscopy Cheng, Hang Zheng, Liming Liu, Nan Huang, Congyuan Xu, Jie Lu, Ye Cui, Xiaoya Xu, Kui Hou, Yuan Tang, Junchuan Zhang, Zhong Li, Jing Ni, Xiaodan Chen, Yanan Peng, Hailin Wang, Hong-Wei J Am Chem Soc [Image: see text] With the development of cryo-electron microscopy (cryo-EM), high-resolution structures of macromolecules can be reconstructed by the single particle method efficiently. However, challenges may still persist during the specimen preparation stage. Specifically, proteins tend to adsorb at the air–water interface and exhibit a preferred orientation in vitreous ice. To overcome these challenges, we have explored dual-affinity graphene (DAG) modified with two different affinity ligands as a supporting material for cryo-EM sample preparation. The ligands can bind to distinct sites on the corresponding tagged particles, which in turn generates various orientation distributions of particles and prevents the adsorption of protein particles onto the air–water interface. As expected, the DAG exhibited high binding specificity and affinity to target macromolecules, resulting in more balanced particle Euler angular distributions compared to single functionalized graphene on two different protein cases, including the SARS -CoV-2 spike glycoprotein. We anticipate that the DAG grids will enable facile and efficient three-dimensional (3D) reconstruction for cryo-EM structural determination, providing a robust and general technique for future studies. American Chemical Society 2023-04-03 /pmc/articles/PMC10103130/ /pubmed/37011903 http://dx.doi.org/10.1021/jacs.3c00659 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Cheng, Hang Zheng, Liming Liu, Nan Huang, Congyuan Xu, Jie Lu, Ye Cui, Xiaoya Xu, Kui Hou, Yuan Tang, Junchuan Zhang, Zhong Li, Jing Ni, Xiaodan Chen, Yanan Peng, Hailin Wang, Hong-Wei Dual-Affinity Graphene Sheets for High-Resolution Cryo-Electron Microscopy |
title | Dual-Affinity
Graphene Sheets for High-Resolution
Cryo-Electron Microscopy |
title_full | Dual-Affinity
Graphene Sheets for High-Resolution
Cryo-Electron Microscopy |
title_fullStr | Dual-Affinity
Graphene Sheets for High-Resolution
Cryo-Electron Microscopy |
title_full_unstemmed | Dual-Affinity
Graphene Sheets for High-Resolution
Cryo-Electron Microscopy |
title_short | Dual-Affinity
Graphene Sheets for High-Resolution
Cryo-Electron Microscopy |
title_sort | dual-affinity
graphene sheets for high-resolution
cryo-electron microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103130/ https://www.ncbi.nlm.nih.gov/pubmed/37011903 http://dx.doi.org/10.1021/jacs.3c00659 |
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