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Permeable Protein-Loaded Polymersome Cascade Nanoreactors by Polymerization-Induced Self-Assembly
[Image: see text] Enzyme loading of polymersomes requires permeability to enable them to interact with the external environment, typically requiring addition of complex functionality to enable porosity. Herein, we describe a synthetic route toward intrinsically permeable polymersomes loaded with fun...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718297/ https://www.ncbi.nlm.nih.gov/pubmed/29226025 http://dx.doi.org/10.1021/acsmacrolett.7b00725 |
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author | Blackman, Lewis D. Varlas, Spyridon Arno, Maria C. Fayter, Alice Gibson, Matthew I. O’Reilly, Rachel K. |
author_facet | Blackman, Lewis D. Varlas, Spyridon Arno, Maria C. Fayter, Alice Gibson, Matthew I. O’Reilly, Rachel K. |
author_sort | Blackman, Lewis D. |
collection | PubMed |
description | [Image: see text] Enzyme loading of polymersomes requires permeability to enable them to interact with the external environment, typically requiring addition of complex functionality to enable porosity. Herein, we describe a synthetic route toward intrinsically permeable polymersomes loaded with functional proteins using initiator-free visible light-mediated polymerization-induced self-assembly (photo-PISA) under mild, aqueous conditions using a commercial monomer. Compartmentalization and retention of protein functionality was demonstrated using green fluorescent protein as a macromolecular chromophore. Catalytic enzyme-loaded vesicles using horseradish peroxidase and glucose oxidase were also prepared and the permeability of the membrane toward their small molecule substrates was revealed for the first time. Finally, the interaction of the compartmentalized enzymes between separate vesicles was validated by means of an enzymatic cascade reaction. These findings have a broad scope as the methodology could be applied for the encapsulation of a large range of macromolecules for advancements in the fields of nanotechnology, biomimicry, and nanomedicine. |
format | Online Article Text |
id | pubmed-5718297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-57182972018-01-03 Permeable Protein-Loaded Polymersome Cascade Nanoreactors by Polymerization-Induced Self-Assembly Blackman, Lewis D. Varlas, Spyridon Arno, Maria C. Fayter, Alice Gibson, Matthew I. O’Reilly, Rachel K. ACS Macro Lett [Image: see text] Enzyme loading of polymersomes requires permeability to enable them to interact with the external environment, typically requiring addition of complex functionality to enable porosity. Herein, we describe a synthetic route toward intrinsically permeable polymersomes loaded with functional proteins using initiator-free visible light-mediated polymerization-induced self-assembly (photo-PISA) under mild, aqueous conditions using a commercial monomer. Compartmentalization and retention of protein functionality was demonstrated using green fluorescent protein as a macromolecular chromophore. Catalytic enzyme-loaded vesicles using horseradish peroxidase and glucose oxidase were also prepared and the permeability of the membrane toward their small molecule substrates was revealed for the first time. Finally, the interaction of the compartmentalized enzymes between separate vesicles was validated by means of an enzymatic cascade reaction. These findings have a broad scope as the methodology could be applied for the encapsulation of a large range of macromolecules for advancements in the fields of nanotechnology, biomimicry, and nanomedicine. American Chemical Society 2017-10-31 2017-11-21 /pmc/articles/PMC5718297/ /pubmed/29226025 http://dx.doi.org/10.1021/acsmacrolett.7b00725 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Blackman, Lewis D. Varlas, Spyridon Arno, Maria C. Fayter, Alice Gibson, Matthew I. O’Reilly, Rachel K. Permeable Protein-Loaded Polymersome Cascade Nanoreactors by Polymerization-Induced Self-Assembly |
title | Permeable Protein-Loaded Polymersome Cascade Nanoreactors
by Polymerization-Induced Self-Assembly |
title_full | Permeable Protein-Loaded Polymersome Cascade Nanoreactors
by Polymerization-Induced Self-Assembly |
title_fullStr | Permeable Protein-Loaded Polymersome Cascade Nanoreactors
by Polymerization-Induced Self-Assembly |
title_full_unstemmed | Permeable Protein-Loaded Polymersome Cascade Nanoreactors
by Polymerization-Induced Self-Assembly |
title_short | Permeable Protein-Loaded Polymersome Cascade Nanoreactors
by Polymerization-Induced Self-Assembly |
title_sort | permeable protein-loaded polymersome cascade nanoreactors
by polymerization-induced self-assembly |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718297/ https://www.ncbi.nlm.nih.gov/pubmed/29226025 http://dx.doi.org/10.1021/acsmacrolett.7b00725 |
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