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Design of multi-scale protein complexes by hierarchical building block fusion

A systematic and robust approach to generating complex protein nanomaterials would have broad utility. We develop a hierarchical approach to designing multi-component protein assemblies from two classes of modular building blocks: designed helical repeat proteins (DHRs) and helical bundle oligomers...

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Autores principales: Hsia, Yang, Mout, Rubul, Sheffler, William, Edman, Natasha I., Vulovic, Ivan, Park, Young-Jun, Redler, Rachel L., Bick, Matthew J., Bera, Asim K., Courbet, Alexis, Kang, Alex, Brunette, T. J., Nattermann, Una, Tsai, Evelyn, Saleem, Ayesha, Chow, Cameron M., Ekiert, Damian, Bhabha, Gira, Veesler, David, Baker, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052403/
https://www.ncbi.nlm.nih.gov/pubmed/33863889
http://dx.doi.org/10.1038/s41467-021-22276-z
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author Hsia, Yang
Mout, Rubul
Sheffler, William
Edman, Natasha I.
Vulovic, Ivan
Park, Young-Jun
Redler, Rachel L.
Bick, Matthew J.
Bera, Asim K.
Courbet, Alexis
Kang, Alex
Brunette, T. J.
Nattermann, Una
Tsai, Evelyn
Saleem, Ayesha
Chow, Cameron M.
Ekiert, Damian
Bhabha, Gira
Veesler, David
Baker, David
author_facet Hsia, Yang
Mout, Rubul
Sheffler, William
Edman, Natasha I.
Vulovic, Ivan
Park, Young-Jun
Redler, Rachel L.
Bick, Matthew J.
Bera, Asim K.
Courbet, Alexis
Kang, Alex
Brunette, T. J.
Nattermann, Una
Tsai, Evelyn
Saleem, Ayesha
Chow, Cameron M.
Ekiert, Damian
Bhabha, Gira
Veesler, David
Baker, David
author_sort Hsia, Yang
collection PubMed
description A systematic and robust approach to generating complex protein nanomaterials would have broad utility. We develop a hierarchical approach to designing multi-component protein assemblies from two classes of modular building blocks: designed helical repeat proteins (DHRs) and helical bundle oligomers (HBs). We first rigidly fuse DHRs to HBs to generate a large library of oligomeric building blocks. We then generate assemblies with cyclic, dihedral, and point group symmetries from these building blocks using architecture guided rigid helical fusion with new software named WORMS. X-ray crystallography and cryo-electron microscopy characterization show that the hierarchical design approach can accurately generate a wide range of assemblies, including a 43 nm diameter icosahedral nanocage. The computational methods and building block sets described here provide a very general route to de novo designed protein nanomaterials.
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spelling pubmed-80524032021-05-11 Design of multi-scale protein complexes by hierarchical building block fusion Hsia, Yang Mout, Rubul Sheffler, William Edman, Natasha I. Vulovic, Ivan Park, Young-Jun Redler, Rachel L. Bick, Matthew J. Bera, Asim K. Courbet, Alexis Kang, Alex Brunette, T. J. Nattermann, Una Tsai, Evelyn Saleem, Ayesha Chow, Cameron M. Ekiert, Damian Bhabha, Gira Veesler, David Baker, David Nat Commun Article A systematic and robust approach to generating complex protein nanomaterials would have broad utility. We develop a hierarchical approach to designing multi-component protein assemblies from two classes of modular building blocks: designed helical repeat proteins (DHRs) and helical bundle oligomers (HBs). We first rigidly fuse DHRs to HBs to generate a large library of oligomeric building blocks. We then generate assemblies with cyclic, dihedral, and point group symmetries from these building blocks using architecture guided rigid helical fusion with new software named WORMS. X-ray crystallography and cryo-electron microscopy characterization show that the hierarchical design approach can accurately generate a wide range of assemblies, including a 43 nm diameter icosahedral nanocage. The computational methods and building block sets described here provide a very general route to de novo designed protein nanomaterials. Nature Publishing Group UK 2021-04-16 /pmc/articles/PMC8052403/ /pubmed/33863889 http://dx.doi.org/10.1038/s41467-021-22276-z 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
Hsia, Yang
Mout, Rubul
Sheffler, William
Edman, Natasha I.
Vulovic, Ivan
Park, Young-Jun
Redler, Rachel L.
Bick, Matthew J.
Bera, Asim K.
Courbet, Alexis
Kang, Alex
Brunette, T. J.
Nattermann, Una
Tsai, Evelyn
Saleem, Ayesha
Chow, Cameron M.
Ekiert, Damian
Bhabha, Gira
Veesler, David
Baker, David
Design of multi-scale protein complexes by hierarchical building block fusion
title Design of multi-scale protein complexes by hierarchical building block fusion
title_full Design of multi-scale protein complexes by hierarchical building block fusion
title_fullStr Design of multi-scale protein complexes by hierarchical building block fusion
title_full_unstemmed Design of multi-scale protein complexes by hierarchical building block fusion
title_short Design of multi-scale protein complexes by hierarchical building block fusion
title_sort design of multi-scale protein complexes by hierarchical building block fusion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052403/
https://www.ncbi.nlm.nih.gov/pubmed/33863889
http://dx.doi.org/10.1038/s41467-021-22276-z
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