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Three-Dimensional Printable Enzymatically Active Plastics
[Image: see text] Here, we describe a facile route to the synthesis of enzymatically active highly fabricable plastics, where the enzyme is an intrinsic component of the material. This is facilitated by the formation of an electrostatically stabilized enzyme–polymer surfactant nanoconstruct, which,...
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/PMC9376927/ https://www.ncbi.nlm.nih.gov/pubmed/35983011 http://dx.doi.org/10.1021/acsapm.1c00845 |
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author | Zhang, William H. Day, Graham J. Zampetakis, Ioannis Carrabba, Michele Zhang, Zhongyang Carter, Ben M. Govan, Norman Jackson, Colin Chen, Menglin Perriman, Adam W. |
author_facet | Zhang, William H. Day, Graham J. Zampetakis, Ioannis Carrabba, Michele Zhang, Zhongyang Carter, Ben M. Govan, Norman Jackson, Colin Chen, Menglin Perriman, Adam W. |
author_sort | Zhang, William H. |
collection | PubMed |
description | [Image: see text] Here, we describe a facile route to the synthesis of enzymatically active highly fabricable plastics, where the enzyme is an intrinsic component of the material. This is facilitated by the formation of an electrostatically stabilized enzyme–polymer surfactant nanoconstruct, which, after lyophilization and melting, affords stable macromolecular dispersions in a wide range of organic solvents. A selection of plastics can then be co-dissolved in the dispersions, which provides a route to bespoke 3D enzyme plastic nanocomposite structures using a wide range of fabrication techniques, including melt electrowriting, casting, and piston-driven 3D printing. The resulting constructs comprising active phosphotriesterase (arPTE) readily detoxify organophosphates with persistent activity over repeated cycles and for long time periods. Moreover, we show that the protein guest molecules, such as arPTE or sfGFP, increase the compressive Young’s modulus of the plastics and that the identity of the biomolecule influences the nanomorphology and mechanical properties of the resulting materials. Overall, we demonstrate that these biologically active nanocomposite plastics are compatible with state-of-the-art 3D fabrication techniques and that the methodology could be readily applied to produce robust and on-demand smart nanomaterial structures. |
format | Online Article Text |
id | pubmed-9376927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93769272022-08-16 Three-Dimensional Printable Enzymatically Active Plastics Zhang, William H. Day, Graham J. Zampetakis, Ioannis Carrabba, Michele Zhang, Zhongyang Carter, Ben M. Govan, Norman Jackson, Colin Chen, Menglin Perriman, Adam W. ACS Appl Polym Mater [Image: see text] Here, we describe a facile route to the synthesis of enzymatically active highly fabricable plastics, where the enzyme is an intrinsic component of the material. This is facilitated by the formation of an electrostatically stabilized enzyme–polymer surfactant nanoconstruct, which, after lyophilization and melting, affords stable macromolecular dispersions in a wide range of organic solvents. A selection of plastics can then be co-dissolved in the dispersions, which provides a route to bespoke 3D enzyme plastic nanocomposite structures using a wide range of fabrication techniques, including melt electrowriting, casting, and piston-driven 3D printing. The resulting constructs comprising active phosphotriesterase (arPTE) readily detoxify organophosphates with persistent activity over repeated cycles and for long time periods. Moreover, we show that the protein guest molecules, such as arPTE or sfGFP, increase the compressive Young’s modulus of the plastics and that the identity of the biomolecule influences the nanomorphology and mechanical properties of the resulting materials. Overall, we demonstrate that these biologically active nanocomposite plastics are compatible with state-of-the-art 3D fabrication techniques and that the methodology could be readily applied to produce robust and on-demand smart nanomaterial structures. American Chemical Society 2021-11-15 2021-12-10 /pmc/articles/PMC9376927/ /pubmed/35983011 http://dx.doi.org/10.1021/acsapm.1c00845 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Zhang, William H. Day, Graham J. Zampetakis, Ioannis Carrabba, Michele Zhang, Zhongyang Carter, Ben M. Govan, Norman Jackson, Colin Chen, Menglin Perriman, Adam W. Three-Dimensional Printable Enzymatically Active Plastics |
title | Three-Dimensional Printable Enzymatically Active Plastics |
title_full | Three-Dimensional Printable Enzymatically Active Plastics |
title_fullStr | Three-Dimensional Printable Enzymatically Active Plastics |
title_full_unstemmed | Three-Dimensional Printable Enzymatically Active Plastics |
title_short | Three-Dimensional Printable Enzymatically Active Plastics |
title_sort | three-dimensional printable enzymatically active plastics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376927/ https://www.ncbi.nlm.nih.gov/pubmed/35983011 http://dx.doi.org/10.1021/acsapm.1c00845 |
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