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Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives

[Image: see text] Supramolecular hydrogels have emerged as a class of promising biomaterials for applications such as drug delivery and tissue engineering. Self-assembling peptides have been well studied for such applications, but low molecular weight (LMW) amino acid-derived gelators have attracted...

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Autores principales: Abraham, Brittany L., Agredo, Pamela, Mensah, Samantha G., Nilsson, Bradley L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776537/
https://www.ncbi.nlm.nih.gov/pubmed/36473193
http://dx.doi.org/10.1021/acs.langmuir.2c01394
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author Abraham, Brittany L.
Agredo, Pamela
Mensah, Samantha G.
Nilsson, Bradley L.
author_facet Abraham, Brittany L.
Agredo, Pamela
Mensah, Samantha G.
Nilsson, Bradley L.
author_sort Abraham, Brittany L.
collection PubMed
description [Image: see text] Supramolecular hydrogels have emerged as a class of promising biomaterials for applications such as drug delivery and tissue engineering. Self-assembling peptides have been well studied for such applications, but low molecular weight (LMW) amino acid-derived gelators have attracted interest as low-cost alternatives with similar emergent properties. Fluorenylmethyloxycarbonyl-phenylalanine (Fmoc-Phe) is one such privileged motif often chosen due to its inherent self-assembly potential. Previously, we developed cationic Fmoc-Phe-DAP gelators that assemble into hydrogel networks in aqueous NaCl solutions of sufficient ionic strength. The chloride anions in these solutions screen the cationic charge of the gelators to enable self-assembly to occur. Herein, we report the effects of varying the anions of sodium salts on the gelation potential, nanoscale morphology, and hydrogel viscoelastic properties of Fmoc-Phe-DAP and two of its fluorinated derivatives, Fmoc-3F-Phe-DAP and Fmoc-F(5)-Phe-DAP. It was observed that both the anion identity and gelator structure had a significant impact on the self-assembly and gelation properties of these derivatives. Changing the anion identity resulted in significant polymorphism of the nanoscale morphology of the assembled states that was dependent on the chemical structure of the gelator. The emergent viscoelastic character of the hydrogel networks was also found to be reliant on the anion identity and gelator structure. These results demonstrate the complex interplay between the gelator and environment that have a profound and often unpredictable impact on both self-assembly properties and emergent viscoelasticity in supramolecular hydrogels formed by LMW compounds. This work also illustrates the current lack of understanding that limits the rational design of potential biomaterials that will be in contact with complex biological fluids and provides motivation for additional research to correlate the chemical structure of LMW gelators with the structure and emergent properties of the resulting supramolecular assemblies as a function of environment.
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spelling pubmed-97765372022-12-23 Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives Abraham, Brittany L. Agredo, Pamela Mensah, Samantha G. Nilsson, Bradley L. Langmuir [Image: see text] Supramolecular hydrogels have emerged as a class of promising biomaterials for applications such as drug delivery and tissue engineering. Self-assembling peptides have been well studied for such applications, but low molecular weight (LMW) amino acid-derived gelators have attracted interest as low-cost alternatives with similar emergent properties. Fluorenylmethyloxycarbonyl-phenylalanine (Fmoc-Phe) is one such privileged motif often chosen due to its inherent self-assembly potential. Previously, we developed cationic Fmoc-Phe-DAP gelators that assemble into hydrogel networks in aqueous NaCl solutions of sufficient ionic strength. The chloride anions in these solutions screen the cationic charge of the gelators to enable self-assembly to occur. Herein, we report the effects of varying the anions of sodium salts on the gelation potential, nanoscale morphology, and hydrogel viscoelastic properties of Fmoc-Phe-DAP and two of its fluorinated derivatives, Fmoc-3F-Phe-DAP and Fmoc-F(5)-Phe-DAP. It was observed that both the anion identity and gelator structure had a significant impact on the self-assembly and gelation properties of these derivatives. Changing the anion identity resulted in significant polymorphism of the nanoscale morphology of the assembled states that was dependent on the chemical structure of the gelator. The emergent viscoelastic character of the hydrogel networks was also found to be reliant on the anion identity and gelator structure. These results demonstrate the complex interplay between the gelator and environment that have a profound and often unpredictable impact on both self-assembly properties and emergent viscoelasticity in supramolecular hydrogels formed by LMW compounds. This work also illustrates the current lack of understanding that limits the rational design of potential biomaterials that will be in contact with complex biological fluids and provides motivation for additional research to correlate the chemical structure of LMW gelators with the structure and emergent properties of the resulting supramolecular assemblies as a function of environment. American Chemical Society 2022-12-06 2022-12-20 /pmc/articles/PMC9776537/ /pubmed/36473193 http://dx.doi.org/10.1021/acs.langmuir.2c01394 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Abraham, Brittany L.
Agredo, Pamela
Mensah, Samantha G.
Nilsson, Bradley L.
Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives
title Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives
title_full Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives
title_fullStr Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives
title_full_unstemmed Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives
title_short Anion Effects on the Supramolecular Self-Assembly of Cationic Phenylalanine Derivatives
title_sort anion effects on the supramolecular self-assembly of cationic phenylalanine derivatives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776537/
https://www.ncbi.nlm.nih.gov/pubmed/36473193
http://dx.doi.org/10.1021/acs.langmuir.2c01394
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