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Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing)
The growing challenge of chronic wounds and antibiotic resistance has spotlighted the potential of dual-function peptides (antimicrobial and wound healing) as novel therapeutic strategies. The investigation aimed to characterize and correlate in silico the physicochemical attributes of these peptide...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487549/ https://www.ncbi.nlm.nih.gov/pubmed/37685896 http://dx.doi.org/10.3390/ijms241713091 |
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author | Trejos, María Aristizabal, Yesid Aragón-Muriel, Alberto Oñate-Garzón, José Liscano, Yamil |
author_facet | Trejos, María Aristizabal, Yesid Aragón-Muriel, Alberto Oñate-Garzón, José Liscano, Yamil |
author_sort | Trejos, María |
collection | PubMed |
description | The growing challenge of chronic wounds and antibiotic resistance has spotlighted the potential of dual-function peptides (antimicrobial and wound healing) as novel therapeutic strategies. The investigation aimed to characterize and correlate in silico the physicochemical attributes of these peptides with their biological activity. We sourced a dataset of 207 such peptides from various peptide databases, followed by a detailed analysis of their physicochemical properties using bioinformatic tools. Utilizing statistical tools like clustering, correlation, and principal component analysis (PCA), patterns and relationships were discerned among these properties. Furthermore, we analyzed the peptides’ functional domains for insights into their potential mechanisms of action. Our findings spotlight peptides in Cluster 2 as efficacious in wound healing, whereas Cluster 1 peptides exhibited pronounced antimicrobial potential. In our study, we identified specific amino acid patterns and peptide families associated with their biological activities, such as the cecropin antimicrobial domain. Additionally, we found the presence of polar amino acids like arginine, cysteine, and lysine, as well as apolar amino acids like glycine, isoleucine, and leucine. These characteristics are crucial for interactions with bacterial membranes and receptors involved in migration, proliferation, angiogenesis, and immunomodulation. While this study provides a groundwork for therapeutic development, translating these findings into practical applications necessitates additional experimental and clinical research. |
format | Online Article Text |
id | pubmed-10487549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104875492023-09-09 Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) Trejos, María Aristizabal, Yesid Aragón-Muriel, Alberto Oñate-Garzón, José Liscano, Yamil Int J Mol Sci Article The growing challenge of chronic wounds and antibiotic resistance has spotlighted the potential of dual-function peptides (antimicrobial and wound healing) as novel therapeutic strategies. The investigation aimed to characterize and correlate in silico the physicochemical attributes of these peptides with their biological activity. We sourced a dataset of 207 such peptides from various peptide databases, followed by a detailed analysis of their physicochemical properties using bioinformatic tools. Utilizing statistical tools like clustering, correlation, and principal component analysis (PCA), patterns and relationships were discerned among these properties. Furthermore, we analyzed the peptides’ functional domains for insights into their potential mechanisms of action. Our findings spotlight peptides in Cluster 2 as efficacious in wound healing, whereas Cluster 1 peptides exhibited pronounced antimicrobial potential. In our study, we identified specific amino acid patterns and peptide families associated with their biological activities, such as the cecropin antimicrobial domain. Additionally, we found the presence of polar amino acids like arginine, cysteine, and lysine, as well as apolar amino acids like glycine, isoleucine, and leucine. These characteristics are crucial for interactions with bacterial membranes and receptors involved in migration, proliferation, angiogenesis, and immunomodulation. While this study provides a groundwork for therapeutic development, translating these findings into practical applications necessitates additional experimental and clinical research. MDPI 2023-08-23 /pmc/articles/PMC10487549/ /pubmed/37685896 http://dx.doi.org/10.3390/ijms241713091 Text en © 2023 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 Trejos, María Aristizabal, Yesid Aragón-Muriel, Alberto Oñate-Garzón, José Liscano, Yamil Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) |
title | Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) |
title_full | Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) |
title_fullStr | Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) |
title_full_unstemmed | Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) |
title_short | Characterization and Classification In Silico of Peptides with Dual Activity (Antimicrobial and Wound Healing) |
title_sort | characterization and classification in silico of peptides with dual activity (antimicrobial and wound healing) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487549/ https://www.ncbi.nlm.nih.gov/pubmed/37685896 http://dx.doi.org/10.3390/ijms241713091 |
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