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Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges

The present work focuses on the computational study of the structural micro-organization of hydrogels based on collagen-like peptides (CLPs) in complex with Rose Bengal (RB). In previous studies, these hydrogels computationally and experimentally demonstrated that when RB was activated by green ligh...

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Autores principales: Rosales-Rojas, Roberto, Zuñiga-Bustos, Matías, Salas-Sepúlveda, Francisca, Galaz-Araya, Constanza, Zamora, Ricardo A., Poblete, Horacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231032/
https://www.ncbi.nlm.nih.gov/pubmed/35745721
http://dx.doi.org/10.3390/pharmaceutics14061148
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author Rosales-Rojas, Roberto
Zuñiga-Bustos, Matías
Salas-Sepúlveda, Francisca
Galaz-Araya, Constanza
Zamora, Ricardo A.
Poblete, Horacio
author_facet Rosales-Rojas, Roberto
Zuñiga-Bustos, Matías
Salas-Sepúlveda, Francisca
Galaz-Araya, Constanza
Zamora, Ricardo A.
Poblete, Horacio
author_sort Rosales-Rojas, Roberto
collection PubMed
description The present work focuses on the computational study of the structural micro-organization of hydrogels based on collagen-like peptides (CLPs) in complex with Rose Bengal (RB). In previous studies, these hydrogels computationally and experimentally demonstrated that when RB was activated by green light, it could generate forms of stable crosslinked structures capable of regenerating biological tissues such as the skin and cornea. Here, we focus on the structural and atomic interactions of two collagen-like peptides (collagen-like peptide I (CLPI), and collagen-like peptide II, (CLPII)) in the presence and absence of RB, highlighting the acquired three-dimensional organization and going deep into the stabilization effect caused by the dye. Our results suggest that the dye could generate a ternary ground-state complex between collagen-like peptide fibers, specifically with positively charged amino acids (Lys in CLPI and Arg in CLPII), thus stabilizing ordered three-dimensional structures. The discoveries generated in this study provide the structural and atomic bases for the subsequent rational development of new synthetic peptides with improved characteristics for applications in the regeneration of biological tissues during photochemical tissue bonding therapies.
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spelling pubmed-92310322022-06-25 Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges Rosales-Rojas, Roberto Zuñiga-Bustos, Matías Salas-Sepúlveda, Francisca Galaz-Araya, Constanza Zamora, Ricardo A. Poblete, Horacio Pharmaceutics Article The present work focuses on the computational study of the structural micro-organization of hydrogels based on collagen-like peptides (CLPs) in complex with Rose Bengal (RB). In previous studies, these hydrogels computationally and experimentally demonstrated that when RB was activated by green light, it could generate forms of stable crosslinked structures capable of regenerating biological tissues such as the skin and cornea. Here, we focus on the structural and atomic interactions of two collagen-like peptides (collagen-like peptide I (CLPI), and collagen-like peptide II, (CLPII)) in the presence and absence of RB, highlighting the acquired three-dimensional organization and going deep into the stabilization effect caused by the dye. Our results suggest that the dye could generate a ternary ground-state complex between collagen-like peptide fibers, specifically with positively charged amino acids (Lys in CLPI and Arg in CLPII), thus stabilizing ordered three-dimensional structures. The discoveries generated in this study provide the structural and atomic bases for the subsequent rational development of new synthetic peptides with improved characteristics for applications in the regeneration of biological tissues during photochemical tissue bonding therapies. MDPI 2022-05-27 /pmc/articles/PMC9231032/ /pubmed/35745721 http://dx.doi.org/10.3390/pharmaceutics14061148 Text en © 2022 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
Rosales-Rojas, Roberto
Zuñiga-Bustos, Matías
Salas-Sepúlveda, Francisca
Galaz-Araya, Constanza
Zamora, Ricardo A.
Poblete, Horacio
Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges
title Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges
title_full Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges
title_fullStr Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges
title_full_unstemmed Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges
title_short Self-Organization Dynamics of Collagen-like Peptides Crosslinking Is Driven by Rose-Bengal-Mediated Electrostatic Bridges
title_sort self-organization dynamics of collagen-like peptides crosslinking is driven by rose-bengal-mediated electrostatic bridges
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231032/
https://www.ncbi.nlm.nih.gov/pubmed/35745721
http://dx.doi.org/10.3390/pharmaceutics14061148
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