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Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic
Peptide-based structures can be designed to yield artificial proteins with specific folding patterns and functions. Template-based assembly of peptide units is one design option, but the use of two orthogonal self-assembly principles, oligonucleotide triple helix and a coiled coil protein domain for...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974474/ https://www.ncbi.nlm.nih.gov/pubmed/27464951 http://dx.doi.org/10.1038/ncomms12294 |
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author | Lou, Chenguang Martos-Maldonado, Manuel C. Madsen, Charlotte S. Thomsen, Rasmus P. Midtgaard, Søren Roi Christensen, Niels Johan Kjems, Jørgen Thulstrup, Peter W. Wengel, Jesper Jensen, Knud J. |
author_facet | Lou, Chenguang Martos-Maldonado, Manuel C. Madsen, Charlotte S. Thomsen, Rasmus P. Midtgaard, Søren Roi Christensen, Niels Johan Kjems, Jørgen Thulstrup, Peter W. Wengel, Jesper Jensen, Knud J. |
author_sort | Lou, Chenguang |
collection | PubMed |
description | Peptide-based structures can be designed to yield artificial proteins with specific folding patterns and functions. Template-based assembly of peptide units is one design option, but the use of two orthogonal self-assembly principles, oligonucleotide triple helix and a coiled coil protein domain formation have never been realized for de novo protein design. Here, we show the applicability of peptide–oligonucleotide conjugates for self-assembly of higher-ordered protein-like structures. The resulting nano-assemblies were characterized by ultraviolet-melting, gel electrophoresis, circular dichroism (CD) spectroscopy, small-angle X-ray scattering and transmission electron microscopy. These studies revealed the formation of the desired triple helix and coiled coil domains at low concentrations, while a dimer of trimers was dominating at high concentration. CD spectroscopy showed an extraordinarily high degree of α-helicity for the peptide moieties in the assemblies. The results validate the use of orthogonal self-assembly principles as a paradigm for de novo protein design. |
format | Online Article Text |
id | pubmed-4974474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49744742016-08-18 Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic Lou, Chenguang Martos-Maldonado, Manuel C. Madsen, Charlotte S. Thomsen, Rasmus P. Midtgaard, Søren Roi Christensen, Niels Johan Kjems, Jørgen Thulstrup, Peter W. Wengel, Jesper Jensen, Knud J. Nat Commun Article Peptide-based structures can be designed to yield artificial proteins with specific folding patterns and functions. Template-based assembly of peptide units is one design option, but the use of two orthogonal self-assembly principles, oligonucleotide triple helix and a coiled coil protein domain formation have never been realized for de novo protein design. Here, we show the applicability of peptide–oligonucleotide conjugates for self-assembly of higher-ordered protein-like structures. The resulting nano-assemblies were characterized by ultraviolet-melting, gel electrophoresis, circular dichroism (CD) spectroscopy, small-angle X-ray scattering and transmission electron microscopy. These studies revealed the formation of the desired triple helix and coiled coil domains at low concentrations, while a dimer of trimers was dominating at high concentration. CD spectroscopy showed an extraordinarily high degree of α-helicity for the peptide moieties in the assemblies. The results validate the use of orthogonal self-assembly principles as a paradigm for de novo protein design. Nature Publishing Group 2016-07-28 /pmc/articles/PMC4974474/ /pubmed/27464951 http://dx.doi.org/10.1038/ncomms12294 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lou, Chenguang Martos-Maldonado, Manuel C. Madsen, Charlotte S. Thomsen, Rasmus P. Midtgaard, Søren Roi Christensen, Niels Johan Kjems, Jørgen Thulstrup, Peter W. Wengel, Jesper Jensen, Knud J. Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
title | Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
title_full | Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
title_fullStr | Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
title_full_unstemmed | Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
title_short | Peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
title_sort | peptide–oligonucleotide conjugates as nanoscale building blocks for assembly of an artificial three-helix protein mimic |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974474/ https://www.ncbi.nlm.nih.gov/pubmed/27464951 http://dx.doi.org/10.1038/ncomms12294 |
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