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Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents

Developing stabilizers that protect proteins from denaturation under stress, and are easy to remove from solutions, is a challenge in protein therapeutics. In this study, micelles made of trehalose, a zwitterionic polymer (poly-sulfobetaine; poly-SPB), and polycaprolactone (PCL) were synthesized by...

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Autores principales: Rajan, Robin, Matsumura, Kazuaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012880/
https://www.ncbi.nlm.nih.gov/pubmed/36926568
http://dx.doi.org/10.1039/d3na00002h
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author Rajan, Robin
Matsumura, Kazuaki
author_facet Rajan, Robin
Matsumura, Kazuaki
author_sort Rajan, Robin
collection PubMed
description Developing stabilizers that protect proteins from denaturation under stress, and are easy to remove from solutions, is a challenge in protein therapeutics. In this study, micelles made of trehalose, a zwitterionic polymer (poly-sulfobetaine; poly-SPB), and polycaprolactone (PCL) were synthesized by a one-pot reversible addition–fragmentation chain-transfer (RAFT) polymerization reaction. The micelles protect lactate dehydrogenase (LDH) and human insulin from denaturation due to stresses like thermal incubation and freezing, and help them retain higher-order structures. Importantly, the protected proteins are readily isolated from the micelles by ultracentrifugation, with over 90% recovery, and almost all enzymatic activity is retained. This suggests the great potential of poly-SPB-based micelles for use in applications requiring protection and removal as required. The micelles may also be used to effectively stabilize protein-based vaccines and drugs.
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spelling pubmed-100128802023-03-15 Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents Rajan, Robin Matsumura, Kazuaki Nanoscale Adv Chemistry Developing stabilizers that protect proteins from denaturation under stress, and are easy to remove from solutions, is a challenge in protein therapeutics. In this study, micelles made of trehalose, a zwitterionic polymer (poly-sulfobetaine; poly-SPB), and polycaprolactone (PCL) were synthesized by a one-pot reversible addition–fragmentation chain-transfer (RAFT) polymerization reaction. The micelles protect lactate dehydrogenase (LDH) and human insulin from denaturation due to stresses like thermal incubation and freezing, and help them retain higher-order structures. Importantly, the protected proteins are readily isolated from the micelles by ultracentrifugation, with over 90% recovery, and almost all enzymatic activity is retained. This suggests the great potential of poly-SPB-based micelles for use in applications requiring protection and removal as required. The micelles may also be used to effectively stabilize protein-based vaccines and drugs. RSC 2023-02-21 /pmc/articles/PMC10012880/ /pubmed/36926568 http://dx.doi.org/10.1039/d3na00002h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Rajan, Robin
Matsumura, Kazuaki
Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
title Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
title_full Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
title_fullStr Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
title_full_unstemmed Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
title_short Design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
title_sort design of self-assembled glycopolymeric zwitterionic micelles as removable protein stabilizing agents
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012880/
https://www.ncbi.nlm.nih.gov/pubmed/36926568
http://dx.doi.org/10.1039/d3na00002h
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