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Designed and biologically active protein lattices
Versatile methods to organize proteins in space are required to enable complex biomaterials, engineered biomolecular scaffolds, cell-free biology, and hybrid nanoscale systems. Here, we demonstrate how the tailored encapsulation of proteins in DNA-based voxels can be combined with programmable assem...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8211860/ https://www.ncbi.nlm.nih.gov/pubmed/34140491 http://dx.doi.org/10.1038/s41467-021-23966-4 |
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author | Wang, Shih-Ting Minevich, Brian Liu, Jianfang Zhang, Honghu Nykypanchuk, Dmytro Byrnes, James Liu, Wu Bershadsky, Lev Liu, Qun Wang, Tong Ren, Gang Gang, Oleg |
author_facet | Wang, Shih-Ting Minevich, Brian Liu, Jianfang Zhang, Honghu Nykypanchuk, Dmytro Byrnes, James Liu, Wu Bershadsky, Lev Liu, Qun Wang, Tong Ren, Gang Gang, Oleg |
author_sort | Wang, Shih-Ting |
collection | PubMed |
description | Versatile methods to organize proteins in space are required to enable complex biomaterials, engineered biomolecular scaffolds, cell-free biology, and hybrid nanoscale systems. Here, we demonstrate how the tailored encapsulation of proteins in DNA-based voxels can be combined with programmable assembly that directs these voxels into biologically functional protein arrays with prescribed and ordered two-dimensional (2D) and three-dimensional (3D) organizations. We apply the presented concept to ferritin, an iron storage protein, and its iron-free analog, apoferritin, in order to form single-layers, double-layers, as well as several types of 3D protein lattices. Our study demonstrates that internal voxel design and inter-voxel encoding can be effectively employed to create protein lattices with designed organization, as confirmed by in situ X-ray scattering and cryo-electron microscopy 3D imaging. The assembled protein arrays maintain structural stability and biological activity in environments relevant for protein functionality. The framework design of the arrays then allows small molecules to access the ferritins and their iron cores and convert them into apoferritin arrays through the release of iron ions. The presented study introduces a platform approach for creating bio-active protein-containing ordered nanomaterials with desired 2D and 3D organizations. |
format | Online Article Text |
id | pubmed-8211860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82118602021-07-01 Designed and biologically active protein lattices Wang, Shih-Ting Minevich, Brian Liu, Jianfang Zhang, Honghu Nykypanchuk, Dmytro Byrnes, James Liu, Wu Bershadsky, Lev Liu, Qun Wang, Tong Ren, Gang Gang, Oleg Nat Commun Article Versatile methods to organize proteins in space are required to enable complex biomaterials, engineered biomolecular scaffolds, cell-free biology, and hybrid nanoscale systems. Here, we demonstrate how the tailored encapsulation of proteins in DNA-based voxels can be combined with programmable assembly that directs these voxels into biologically functional protein arrays with prescribed and ordered two-dimensional (2D) and three-dimensional (3D) organizations. We apply the presented concept to ferritin, an iron storage protein, and its iron-free analog, apoferritin, in order to form single-layers, double-layers, as well as several types of 3D protein lattices. Our study demonstrates that internal voxel design and inter-voxel encoding can be effectively employed to create protein lattices with designed organization, as confirmed by in situ X-ray scattering and cryo-electron microscopy 3D imaging. The assembled protein arrays maintain structural stability and biological activity in environments relevant for protein functionality. The framework design of the arrays then allows small molecules to access the ferritins and their iron cores and convert them into apoferritin arrays through the release of iron ions. The presented study introduces a platform approach for creating bio-active protein-containing ordered nanomaterials with desired 2D and 3D organizations. Nature Publishing Group UK 2021-06-17 /pmc/articles/PMC8211860/ /pubmed/34140491 http://dx.doi.org/10.1038/s41467-021-23966-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Shih-Ting Minevich, Brian Liu, Jianfang Zhang, Honghu Nykypanchuk, Dmytro Byrnes, James Liu, Wu Bershadsky, Lev Liu, Qun Wang, Tong Ren, Gang Gang, Oleg Designed and biologically active protein lattices |
title | Designed and biologically active protein lattices |
title_full | Designed and biologically active protein lattices |
title_fullStr | Designed and biologically active protein lattices |
title_full_unstemmed | Designed and biologically active protein lattices |
title_short | Designed and biologically active protein lattices |
title_sort | designed and biologically active protein lattices |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8211860/ https://www.ncbi.nlm.nih.gov/pubmed/34140491 http://dx.doi.org/10.1038/s41467-021-23966-4 |
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