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Protein Hydration in a Bioprotecting Mixture
We combined broad-band depolarized light scattering and infrared spectroscopies to study the properties of hydration water in a lysozyme-trehalose aqueous solution, where trehalose is present above the concentration threshold (30% in weight) relevant for biopreservation. The joint use of the two dif...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537178/ https://www.ncbi.nlm.nih.gov/pubmed/34685367 http://dx.doi.org/10.3390/life11100995 |
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author | Corezzi, Silvia Bracco, Brenda Sassi, Paola Paolantoni, Marco Comez, Lucia |
author_facet | Corezzi, Silvia Bracco, Brenda Sassi, Paola Paolantoni, Marco Comez, Lucia |
author_sort | Corezzi, Silvia |
collection | PubMed |
description | We combined broad-band depolarized light scattering and infrared spectroscopies to study the properties of hydration water in a lysozyme-trehalose aqueous solution, where trehalose is present above the concentration threshold (30% in weight) relevant for biopreservation. The joint use of the two different techniques, which were sensitive to inter-and intra-molecular degrees of freedom, shed new light on the molecular mechanism underlying the interaction between the three species in the mixture. Thanks to the comparison with the binary solution cases, we were able to show that, under the investigated conditions, the protein, through preferential hydration, remains strongly hydrated even in the ternary mixture. This supported the water entrapment scenario, for which a certain amount of water between protein and sugar protects the biomolecule from damage caused by external agents. |
format | Online Article Text |
id | pubmed-8537178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85371782021-10-24 Protein Hydration in a Bioprotecting Mixture Corezzi, Silvia Bracco, Brenda Sassi, Paola Paolantoni, Marco Comez, Lucia Life (Basel) Article We combined broad-band depolarized light scattering and infrared spectroscopies to study the properties of hydration water in a lysozyme-trehalose aqueous solution, where trehalose is present above the concentration threshold (30% in weight) relevant for biopreservation. The joint use of the two different techniques, which were sensitive to inter-and intra-molecular degrees of freedom, shed new light on the molecular mechanism underlying the interaction between the three species in the mixture. Thanks to the comparison with the binary solution cases, we were able to show that, under the investigated conditions, the protein, through preferential hydration, remains strongly hydrated even in the ternary mixture. This supported the water entrapment scenario, for which a certain amount of water between protein and sugar protects the biomolecule from damage caused by external agents. MDPI 2021-09-22 /pmc/articles/PMC8537178/ /pubmed/34685367 http://dx.doi.org/10.3390/life11100995 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Corezzi, Silvia Bracco, Brenda Sassi, Paola Paolantoni, Marco Comez, Lucia Protein Hydration in a Bioprotecting Mixture |
title | Protein Hydration in a Bioprotecting Mixture |
title_full | Protein Hydration in a Bioprotecting Mixture |
title_fullStr | Protein Hydration in a Bioprotecting Mixture |
title_full_unstemmed | Protein Hydration in a Bioprotecting Mixture |
title_short | Protein Hydration in a Bioprotecting Mixture |
title_sort | protein hydration in a bioprotecting mixture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537178/ https://www.ncbi.nlm.nih.gov/pubmed/34685367 http://dx.doi.org/10.3390/life11100995 |
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