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Solid-phase synthesis of protein-polymers on reversible immobilization supports

Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds. Full access to abiotic/biotic synthetic diversity first occurred when chemistry was developed to grow nucleic acids and peptides from reversibly immobilized precursors. Protein–polymer conjugates,...

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Autores principales: Murata, Hironobu, Carmali, Sheiliza, Baker, Stefanie L., Matyjaszewski, Krzysztof, Russell, Alan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829226/
https://www.ncbi.nlm.nih.gov/pubmed/29487296
http://dx.doi.org/10.1038/s41467-018-03153-8
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author Murata, Hironobu
Carmali, Sheiliza
Baker, Stefanie L.
Matyjaszewski, Krzysztof
Russell, Alan J.
author_facet Murata, Hironobu
Carmali, Sheiliza
Baker, Stefanie L.
Matyjaszewski, Krzysztof
Russell, Alan J.
author_sort Murata, Hironobu
collection PubMed
description Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds. Full access to abiotic/biotic synthetic diversity first occurred when chemistry was developed to grow nucleic acids and peptides from reversibly immobilized precursors. Protein–polymer conjugates, however, have always been synthesized in solution in multi-step, multi-day processes that couple innovative chemistry with challenging purification. Here we report the generation of protein–polymer hybrids synthesized by protein-ATRP on reversible immobilization supports (PARIS). We utilized modified agarose beads to covalently and reversibly couple to proteins in amino-specific reactions. We then modified reversibly immobilized proteins with protein-reactive ATRP initiators and, after ATRP, we released and analyzed the protein polymers. The activity and stability of PARIS-synthesized and solution-synthesized conjugates demonstrated that PARIS was an effective, rapid, and simple method to generate protein–polymer conjugates. Automation of PARIS significantly reduced synthesis/purification timelines, thereby opening a path to changing how to generate protein–polymer conjugates.
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spelling pubmed-58292262018-03-02 Solid-phase synthesis of protein-polymers on reversible immobilization supports Murata, Hironobu Carmali, Sheiliza Baker, Stefanie L. Matyjaszewski, Krzysztof Russell, Alan J. Nat Commun Article Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds. Full access to abiotic/biotic synthetic diversity first occurred when chemistry was developed to grow nucleic acids and peptides from reversibly immobilized precursors. Protein–polymer conjugates, however, have always been synthesized in solution in multi-step, multi-day processes that couple innovative chemistry with challenging purification. Here we report the generation of protein–polymer hybrids synthesized by protein-ATRP on reversible immobilization supports (PARIS). We utilized modified agarose beads to covalently and reversibly couple to proteins in amino-specific reactions. We then modified reversibly immobilized proteins with protein-reactive ATRP initiators and, after ATRP, we released and analyzed the protein polymers. The activity and stability of PARIS-synthesized and solution-synthesized conjugates demonstrated that PARIS was an effective, rapid, and simple method to generate protein–polymer conjugates. Automation of PARIS significantly reduced synthesis/purification timelines, thereby opening a path to changing how to generate protein–polymer conjugates. Nature Publishing Group UK 2018-02-27 /pmc/articles/PMC5829226/ /pubmed/29487296 http://dx.doi.org/10.1038/s41467-018-03153-8 Text en © The Author(s) 2018 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
Murata, Hironobu
Carmali, Sheiliza
Baker, Stefanie L.
Matyjaszewski, Krzysztof
Russell, Alan J.
Solid-phase synthesis of protein-polymers on reversible immobilization supports
title Solid-phase synthesis of protein-polymers on reversible immobilization supports
title_full Solid-phase synthesis of protein-polymers on reversible immobilization supports
title_fullStr Solid-phase synthesis of protein-polymers on reversible immobilization supports
title_full_unstemmed Solid-phase synthesis of protein-polymers on reversible immobilization supports
title_short Solid-phase synthesis of protein-polymers on reversible immobilization supports
title_sort solid-phase synthesis of protein-polymers on reversible immobilization supports
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829226/
https://www.ncbi.nlm.nih.gov/pubmed/29487296
http://dx.doi.org/10.1038/s41467-018-03153-8
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