Cargando…
Plasticizing Effects of Polyamines in Protein-Based Films
Zeta potential and nanoparticle size were determined on film forming solutions of native and heat-denatured proteins of bitter vetch as a function of pH and of different concentrations of the polyamines spermidine and spermine, both in the absence and presence of the plasticizer glycerol. Our result...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454938/ https://www.ncbi.nlm.nih.gov/pubmed/28489025 http://dx.doi.org/10.3390/ijms18051026 |
_version_ | 1783240941756219392 |
---|---|
author | Sabbah, Mohammed Di Pierro, Prospero Giosafatto, C. Valeria L. Esposito, Marilena Mariniello, Loredana Regalado-Gonzales, Carlos Porta, Raffaele |
author_facet | Sabbah, Mohammed Di Pierro, Prospero Giosafatto, C. Valeria L. Esposito, Marilena Mariniello, Loredana Regalado-Gonzales, Carlos Porta, Raffaele |
author_sort | Sabbah, Mohammed |
collection | PubMed |
description | Zeta potential and nanoparticle size were determined on film forming solutions of native and heat-denatured proteins of bitter vetch as a function of pH and of different concentrations of the polyamines spermidine and spermine, both in the absence and presence of the plasticizer glycerol. Our results showed that both polyamines decreased the negative zeta potential of all samples under pH 8.0 as a consequence of their ionic interaction with proteins. At the same time, they enhanced the dimension of nanoparticles under pH 8.0 as a result of macromolecular aggregations. By using native protein solutions, handleable films were obtained only from samples containing either a minimum of 33 mM glycerol or 4 mM spermidine, or both compounds together at lower glycerol concentrations. However, 2 mM spermidine was sufficient to obtain handleable film by using heat-treated samples without glycerol. Conversely, brittle materials were obtained by spermine alone, thus indicating that only spermidine was able to act as an ionic plasticizer. Lastly, both polyamines, mainly spermine, were found able to act as “glycerol-like” plasticizers at concentrations higher than 5 mM under experimental conditions at which their amino groups are undissociated. Our findings open new perspectives in obtaining protein-based films by using aliphatic polycations as components. |
format | Online Article Text |
id | pubmed-5454938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-54549382017-06-08 Plasticizing Effects of Polyamines in Protein-Based Films Sabbah, Mohammed Di Pierro, Prospero Giosafatto, C. Valeria L. Esposito, Marilena Mariniello, Loredana Regalado-Gonzales, Carlos Porta, Raffaele Int J Mol Sci Article Zeta potential and nanoparticle size were determined on film forming solutions of native and heat-denatured proteins of bitter vetch as a function of pH and of different concentrations of the polyamines spermidine and spermine, both in the absence and presence of the plasticizer glycerol. Our results showed that both polyamines decreased the negative zeta potential of all samples under pH 8.0 as a consequence of their ionic interaction with proteins. At the same time, they enhanced the dimension of nanoparticles under pH 8.0 as a result of macromolecular aggregations. By using native protein solutions, handleable films were obtained only from samples containing either a minimum of 33 mM glycerol or 4 mM spermidine, or both compounds together at lower glycerol concentrations. However, 2 mM spermidine was sufficient to obtain handleable film by using heat-treated samples without glycerol. Conversely, brittle materials were obtained by spermine alone, thus indicating that only spermidine was able to act as an ionic plasticizer. Lastly, both polyamines, mainly spermine, were found able to act as “glycerol-like” plasticizers at concentrations higher than 5 mM under experimental conditions at which their amino groups are undissociated. Our findings open new perspectives in obtaining protein-based films by using aliphatic polycations as components. MDPI 2017-05-10 /pmc/articles/PMC5454938/ /pubmed/28489025 http://dx.doi.org/10.3390/ijms18051026 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sabbah, Mohammed Di Pierro, Prospero Giosafatto, C. Valeria L. Esposito, Marilena Mariniello, Loredana Regalado-Gonzales, Carlos Porta, Raffaele Plasticizing Effects of Polyamines in Protein-Based Films |
title | Plasticizing Effects of Polyamines in Protein-Based Films |
title_full | Plasticizing Effects of Polyamines in Protein-Based Films |
title_fullStr | Plasticizing Effects of Polyamines in Protein-Based Films |
title_full_unstemmed | Plasticizing Effects of Polyamines in Protein-Based Films |
title_short | Plasticizing Effects of Polyamines in Protein-Based Films |
title_sort | plasticizing effects of polyamines in protein-based films |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454938/ https://www.ncbi.nlm.nih.gov/pubmed/28489025 http://dx.doi.org/10.3390/ijms18051026 |
work_keys_str_mv | AT sabbahmohammed plasticizingeffectsofpolyaminesinproteinbasedfilms AT dipierroprospero plasticizingeffectsofpolyaminesinproteinbasedfilms AT giosafattocvalerial plasticizingeffectsofpolyaminesinproteinbasedfilms AT espositomarilena plasticizingeffectsofpolyaminesinproteinbasedfilms AT marinielloloredana plasticizingeffectsofpolyaminesinproteinbasedfilms AT regaladogonzalescarlos plasticizingeffectsofpolyaminesinproteinbasedfilms AT portaraffaele plasticizingeffectsofpolyaminesinproteinbasedfilms |