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Heterogeneous Charged Complexes of Random Copolymers for the Segregation of Organic Molecules
[Image: see text] Nature harnesses the disorder of intrinsically disordered proteins to organize enzymes and biopolymers into membraneless organelles. The heterogeneous nature of synthetic random copolymers with charged, polar, and hydrophobic groups has been exploited to mimic intrinsically disorde...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161480/ https://www.ncbi.nlm.nih.gov/pubmed/34079903 http://dx.doi.org/10.1021/acscentsci.1c00119 |
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author | Wang, Jeremy Waltmann, Curt Umana-Kossio, Han Olvera de la Cruz, Monica Torkelson, John M. |
author_facet | Wang, Jeremy Waltmann, Curt Umana-Kossio, Han Olvera de la Cruz, Monica Torkelson, John M. |
author_sort | Wang, Jeremy |
collection | PubMed |
description | [Image: see text] Nature harnesses the disorder of intrinsically disordered proteins to organize enzymes and biopolymers into membraneless organelles. The heterogeneous nature of synthetic random copolymers with charged, polar, and hydrophobic groups has been exploited to mimic intrinsically disordered proteins, forming complexes with enzymatically active proteins and delivering them into nonbiological environments. Here, the properties of polyelectrolyte complexes composed of two random copolymer polyelectrolytes are studied experimentally and via simulation with the aim of exploiting such complexes for segregating organic molecules from water. The anionic polyelectrolyte contains hydrophilic and hydrophobic side chains and forms self-assembled hydrophobic domains. The cationic polymer is a high-molecular-weight copolymer of hydrophilic and charged side groups and acts as a flocculant. We find that the polyelectrolyte complexes obtained with this anionic and cationic random copolymer system are capable of absorbing small cationic, anionic, and hydrophobic organic molecules, including perfluorooctanoic acid, a compound of great environmental and toxicologic concern. Importantly, these macroscopic complexes can be easily removed from water, thereby providing a simple approach for organic contaminant removal in aqueous media. MARTINI and coarse-grained molecular dynamics simulations explore how the microscale heterogeneity of these random copolymer complexes relates to their segregation functionality. |
format | Online Article Text |
id | pubmed-8161480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81614802021-06-01 Heterogeneous Charged Complexes of Random Copolymers for the Segregation of Organic Molecules Wang, Jeremy Waltmann, Curt Umana-Kossio, Han Olvera de la Cruz, Monica Torkelson, John M. ACS Cent Sci [Image: see text] Nature harnesses the disorder of intrinsically disordered proteins to organize enzymes and biopolymers into membraneless organelles. The heterogeneous nature of synthetic random copolymers with charged, polar, and hydrophobic groups has been exploited to mimic intrinsically disordered proteins, forming complexes with enzymatically active proteins and delivering them into nonbiological environments. Here, the properties of polyelectrolyte complexes composed of two random copolymer polyelectrolytes are studied experimentally and via simulation with the aim of exploiting such complexes for segregating organic molecules from water. The anionic polyelectrolyte contains hydrophilic and hydrophobic side chains and forms self-assembled hydrophobic domains. The cationic polymer is a high-molecular-weight copolymer of hydrophilic and charged side groups and acts as a flocculant. We find that the polyelectrolyte complexes obtained with this anionic and cationic random copolymer system are capable of absorbing small cationic, anionic, and hydrophobic organic molecules, including perfluorooctanoic acid, a compound of great environmental and toxicologic concern. Importantly, these macroscopic complexes can be easily removed from water, thereby providing a simple approach for organic contaminant removal in aqueous media. MARTINI and coarse-grained molecular dynamics simulations explore how the microscale heterogeneity of these random copolymer complexes relates to their segregation functionality. American Chemical Society 2021-05-04 2021-05-26 /pmc/articles/PMC8161480/ /pubmed/34079903 http://dx.doi.org/10.1021/acscentsci.1c00119 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Wang, Jeremy Waltmann, Curt Umana-Kossio, Han Olvera de la Cruz, Monica Torkelson, John M. Heterogeneous Charged Complexes of Random Copolymers for the Segregation of Organic Molecules |
title | Heterogeneous Charged Complexes of Random Copolymers
for the Segregation of Organic Molecules |
title_full | Heterogeneous Charged Complexes of Random Copolymers
for the Segregation of Organic Molecules |
title_fullStr | Heterogeneous Charged Complexes of Random Copolymers
for the Segregation of Organic Molecules |
title_full_unstemmed | Heterogeneous Charged Complexes of Random Copolymers
for the Segregation of Organic Molecules |
title_short | Heterogeneous Charged Complexes of Random Copolymers
for the Segregation of Organic Molecules |
title_sort | heterogeneous charged complexes of random copolymers
for the segregation of organic molecules |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161480/ https://www.ncbi.nlm.nih.gov/pubmed/34079903 http://dx.doi.org/10.1021/acscentsci.1c00119 |
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