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Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan

[Image: see text] We use two-dimensional infrared spectroscopy to study the interactions between the amide and carboxylate anion groups of hyaluronan polymers at neutral pH. The spectra reveal the presence of intrachain hydrogen bonds between the amide and carboxylate anion groups in aqueous solutio...

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Autores principales: Giubertoni, Giulia, Koenderink, Gijsje H., Bakker, Huib J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767362/
https://www.ncbi.nlm.nih.gov/pubmed/31478665
http://dx.doi.org/10.1021/acs.jpca.9b06462
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author Giubertoni, Giulia
Koenderink, Gijsje H.
Bakker, Huib J.
author_facet Giubertoni, Giulia
Koenderink, Gijsje H.
Bakker, Huib J.
author_sort Giubertoni, Giulia
collection PubMed
description [Image: see text] We use two-dimensional infrared spectroscopy to study the interactions between the amide and carboxylate anion groups of hyaluronan polymers at neutral pH. The spectra reveal the presence of intrachain hydrogen bonds between the amide and carboxylate anion groups in aqueous solution. We determine the relative orientation of the amide and carboxylate anion groups when forming this hydrogen bond and quantify the fraction of amide groups that participate in hydrogen bonding. We find that a variation of the pH and/or temperature has a negligible effect on this fraction, whereas the persistence length of the hyaluronan chains and the associated viscosity of hyaluronan solutions are known to change significantly. We conclude that the hydrogen bonding between the amide and carboxylate anion groups does not significantly contribute to the chain rigidity of hyaluronan polymers.
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spelling pubmed-67673622019-10-01 Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan Giubertoni, Giulia Koenderink, Gijsje H. Bakker, Huib J. J Phys Chem A [Image: see text] We use two-dimensional infrared spectroscopy to study the interactions between the amide and carboxylate anion groups of hyaluronan polymers at neutral pH. The spectra reveal the presence of intrachain hydrogen bonds between the amide and carboxylate anion groups in aqueous solution. We determine the relative orientation of the amide and carboxylate anion groups when forming this hydrogen bond and quantify the fraction of amide groups that participate in hydrogen bonding. We find that a variation of the pH and/or temperature has a negligible effect on this fraction, whereas the persistence length of the hyaluronan chains and the associated viscosity of hyaluronan solutions are known to change significantly. We conclude that the hydrogen bonding between the amide and carboxylate anion groups does not significantly contribute to the chain rigidity of hyaluronan polymers. American Chemical Society 2019-09-03 2019-09-26 /pmc/articles/PMC6767362/ /pubmed/31478665 http://dx.doi.org/10.1021/acs.jpca.9b06462 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Giubertoni, Giulia
Koenderink, Gijsje H.
Bakker, Huib J.
Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan
title Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan
title_full Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan
title_fullStr Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan
title_full_unstemmed Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan
title_short Direct Observation of Intrachain Hydrogen Bonds in Aqueous Hyaluronan
title_sort direct observation of intrachain hydrogen bonds in aqueous hyaluronan
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767362/
https://www.ncbi.nlm.nih.gov/pubmed/31478665
http://dx.doi.org/10.1021/acs.jpca.9b06462
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