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Metal ion–regulated assembly of designed modular protein cages
Coiled-coil (CC) dimers are versatile, customizable building modules for the design of diverse protein architectures unknown in nature. Incorporation of dynamic self-assembly, regulated by a selected chemical signal, represents an important challenge in the construction of functional polypeptide nan...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205593/ https://www.ncbi.nlm.nih.gov/pubmed/35714197 http://dx.doi.org/10.1126/sciadv.abm8243 |
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author | Aupič, Jana Lapenta, Fabio Strmšek, Žiga Merljak, Estera Plaper, Tjaša Jerala, Roman |
author_facet | Aupič, Jana Lapenta, Fabio Strmšek, Žiga Merljak, Estera Plaper, Tjaša Jerala, Roman |
author_sort | Aupič, Jana |
collection | PubMed |
description | Coiled-coil (CC) dimers are versatile, customizable building modules for the design of diverse protein architectures unknown in nature. Incorporation of dynamic self-assembly, regulated by a selected chemical signal, represents an important challenge in the construction of functional polypeptide nanostructures. Here, we engineered metal binding sites to render an orthogonal set of CC heterodimers Zn(II)-responsive as a generally applicable principle. The designed peptides assemble into CC heterodimers only in the presence of Zn(II) ions, reversibly dissociate by metal ion sequestration, and additionally act as pH switches, with low pH triggering disassembly. The developed Zn(II)-responsive CC set is used to construct programmable folding of CC-based nanostructures, from protein triangles to a two-chain bipyramidal protein cage that closes and opens depending on the metal ion. This demonstrates that dynamic self-assembly can be designed into CC-based protein cages by incorporation of metal ion–responsive CC building modules that act as conformational switches and that could also be used in other contexts. |
format | Online Article Text |
id | pubmed-9205593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92055932022-06-29 Metal ion–regulated assembly of designed modular protein cages Aupič, Jana Lapenta, Fabio Strmšek, Žiga Merljak, Estera Plaper, Tjaša Jerala, Roman Sci Adv Physical and Materials Sciences Coiled-coil (CC) dimers are versatile, customizable building modules for the design of diverse protein architectures unknown in nature. Incorporation of dynamic self-assembly, regulated by a selected chemical signal, represents an important challenge in the construction of functional polypeptide nanostructures. Here, we engineered metal binding sites to render an orthogonal set of CC heterodimers Zn(II)-responsive as a generally applicable principle. The designed peptides assemble into CC heterodimers only in the presence of Zn(II) ions, reversibly dissociate by metal ion sequestration, and additionally act as pH switches, with low pH triggering disassembly. The developed Zn(II)-responsive CC set is used to construct programmable folding of CC-based nanostructures, from protein triangles to a two-chain bipyramidal protein cage that closes and opens depending on the metal ion. This demonstrates that dynamic self-assembly can be designed into CC-based protein cages by incorporation of metal ion–responsive CC building modules that act as conformational switches and that could also be used in other contexts. American Association for the Advancement of Science 2022-06-17 /pmc/articles/PMC9205593/ /pubmed/35714197 http://dx.doi.org/10.1126/sciadv.abm8243 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Physical and Materials Sciences Aupič, Jana Lapenta, Fabio Strmšek, Žiga Merljak, Estera Plaper, Tjaša Jerala, Roman Metal ion–regulated assembly of designed modular protein cages |
title | Metal ion–regulated assembly of designed modular protein cages |
title_full | Metal ion–regulated assembly of designed modular protein cages |
title_fullStr | Metal ion–regulated assembly of designed modular protein cages |
title_full_unstemmed | Metal ion–regulated assembly of designed modular protein cages |
title_short | Metal ion–regulated assembly of designed modular protein cages |
title_sort | metal ion–regulated assembly of designed modular protein cages |
topic | Physical and Materials Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205593/ https://www.ncbi.nlm.nih.gov/pubmed/35714197 http://dx.doi.org/10.1126/sciadv.abm8243 |
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