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Geometrical frustration yields fiber formation in self-assembly
Controlling the self-assembly of supramolecular structures is vital for living cells, and a central challenge for engineering at the nano- and microscales [1, 2]. Nevertheless, even particles without optimized shapes can robustly form well-defined morphologies. This is the case in numerous medical c...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669487/ https://www.ncbi.nlm.nih.gov/pubmed/29109755 http://dx.doi.org/10.1038/nphys4184 |
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author | Lenz, Martin Witten, Thomas A. |
author_facet | Lenz, Martin Witten, Thomas A. |
author_sort | Lenz, Martin |
collection | PubMed |
description | Controlling the self-assembly of supramolecular structures is vital for living cells, and a central challenge for engineering at the nano- and microscales [1, 2]. Nevertheless, even particles without optimized shapes can robustly form well-defined morphologies. This is the case in numerous medical conditions where normally soluble proteins aggregate into fibers [3, 4]. Beyond the diversity of molecular mechanisms involved [5, 6], we propose that fibers generically arise from the aggregation of irregular particles with short-range interactions. Using a minimal model of ill-fitting, sticky particles, we demonstrate robust fiber formation for a variety of particle shapes and aggregation conditions. Geometrical frustration plays a crucial role in this process, and accounts for the range of parameters in which fibers form as well as for their metastable character. |
format | Online Article Text |
id | pubmed-5669487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-56694872018-01-03 Geometrical frustration yields fiber formation in self-assembly Lenz, Martin Witten, Thomas A. Nat Phys Article Controlling the self-assembly of supramolecular structures is vital for living cells, and a central challenge for engineering at the nano- and microscales [1, 2]. Nevertheless, even particles without optimized shapes can robustly form well-defined morphologies. This is the case in numerous medical conditions where normally soluble proteins aggregate into fibers [3, 4]. Beyond the diversity of molecular mechanisms involved [5, 6], we propose that fibers generically arise from the aggregation of irregular particles with short-range interactions. Using a minimal model of ill-fitting, sticky particles, we demonstrate robust fiber formation for a variety of particle shapes and aggregation conditions. Geometrical frustration plays a crucial role in this process, and accounts for the range of parameters in which fibers form as well as for their metastable character. 2017-07-03 2017-11 /pmc/articles/PMC5669487/ /pubmed/29109755 http://dx.doi.org/10.1038/nphys4184 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lenz, Martin Witten, Thomas A. Geometrical frustration yields fiber formation in self-assembly |
title | Geometrical frustration yields fiber formation in self-assembly |
title_full | Geometrical frustration yields fiber formation in self-assembly |
title_fullStr | Geometrical frustration yields fiber formation in self-assembly |
title_full_unstemmed | Geometrical frustration yields fiber formation in self-assembly |
title_short | Geometrical frustration yields fiber formation in self-assembly |
title_sort | geometrical frustration yields fiber formation in self-assembly |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669487/ https://www.ncbi.nlm.nih.gov/pubmed/29109755 http://dx.doi.org/10.1038/nphys4184 |
work_keys_str_mv | AT lenzmartin geometricalfrustrationyieldsfiberformationinselfassembly AT wittenthomasa geometricalfrustrationyieldsfiberformationinselfassembly |