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Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions
Topological structures of bio-architectonics and bio-interfaces play major roles in maintaining the normal functions of organs, tissues, extracellular matrix, and cells. In-depth understanding of natural self-assembly mechanisms and mimicking functional structures provide us opportunities to artific...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668255/ https://www.ncbi.nlm.nih.gov/pubmed/29097677 http://dx.doi.org/10.1038/s41467-017-01296-8 |
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author | Li, Li-Li Qiao, Sheng-Lin Liu, Wei-Jiao Ma, Yang Wan, Dong Pan, Jie Wang, Hao |
author_facet | Li, Li-Li Qiao, Sheng-Lin Liu, Wei-Jiao Ma, Yang Wan, Dong Pan, Jie Wang, Hao |
author_sort | Li, Li-Li |
collection | PubMed |
description | Topological structures of bio-architectonics and bio-interfaces play major roles in maintaining the normal functions of organs, tissues, extracellular matrix, and cells. In-depth understanding of natural self-assembly mechanisms and mimicking functional structures provide us opportunities to artificially control the natural assemblies and their biofunctions. Here, we report an intracellular enzyme-catalyzed polymerization approach for efficient synthesis of polypeptides and in situ construction of topology-controlled nanostructures. We reveal that the phase behavior and topological structure of polypeptides are encoded in monomeric peptide sequences. Next, we elucidate the relationship between polymerization dynamics and their temperature-dependent topological transition in biological conditions. Importantly, the linearly grown elastin-like polypeptides are biocompatible and aggregate into nanoparticles that exhibit significant molecular accumulation and retention effects. However, 3D gel-like structures with thermo-induced multi-directional traction interfere with cellular fates. These findings allow us to exploit new nanomaterials in living subjects for biomedical applications. |
format | Online Article Text |
id | pubmed-5668255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56682552017-11-07 Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions Li, Li-Li Qiao, Sheng-Lin Liu, Wei-Jiao Ma, Yang Wan, Dong Pan, Jie Wang, Hao Nat Commun Article Topological structures of bio-architectonics and bio-interfaces play major roles in maintaining the normal functions of organs, tissues, extracellular matrix, and cells. In-depth understanding of natural self-assembly mechanisms and mimicking functional structures provide us opportunities to artificially control the natural assemblies and their biofunctions. Here, we report an intracellular enzyme-catalyzed polymerization approach for efficient synthesis of polypeptides and in situ construction of topology-controlled nanostructures. We reveal that the phase behavior and topological structure of polypeptides are encoded in monomeric peptide sequences. Next, we elucidate the relationship between polymerization dynamics and their temperature-dependent topological transition in biological conditions. Importantly, the linearly grown elastin-like polypeptides are biocompatible and aggregate into nanoparticles that exhibit significant molecular accumulation and retention effects. However, 3D gel-like structures with thermo-induced multi-directional traction interfere with cellular fates. These findings allow us to exploit new nanomaterials in living subjects for biomedical applications. Nature Publishing Group UK 2017-11-02 /pmc/articles/PMC5668255/ /pubmed/29097677 http://dx.doi.org/10.1038/s41467-017-01296-8 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Li, Li-Li Qiao, Sheng-Lin Liu, Wei-Jiao Ma, Yang Wan, Dong Pan, Jie Wang, Hao Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
title | Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
title_full | Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
title_fullStr | Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
title_full_unstemmed | Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
title_short | Intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
title_sort | intracellular construction of topology-controlled polypeptide nanostructures with diverse biological functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668255/ https://www.ncbi.nlm.nih.gov/pubmed/29097677 http://dx.doi.org/10.1038/s41467-017-01296-8 |
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