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Structure-Based Design of Peptides Targeting VEGF/VEGFRs
Vascular endothelial growth factor (VEGF) and its receptors (VEGFRs) play a main role in the regulation of angiogenesis and lymphangiogenesis. Furthermore, they are implicated in the onset of several diseases such as rheumatoid arthritis, degenerative eye conditions, tumor growth, ulcers and ischemi...
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/PMC10302803/ https://www.ncbi.nlm.nih.gov/pubmed/37375798 http://dx.doi.org/10.3390/ph16060851 |
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author | Di Stasi, Rossella De Rosa, Lucia D’Andrea, Luca Domenico |
author_facet | Di Stasi, Rossella De Rosa, Lucia D’Andrea, Luca Domenico |
author_sort | Di Stasi, Rossella |
collection | PubMed |
description | Vascular endothelial growth factor (VEGF) and its receptors (VEGFRs) play a main role in the regulation of angiogenesis and lymphangiogenesis. Furthermore, they are implicated in the onset of several diseases such as rheumatoid arthritis, degenerative eye conditions, tumor growth, ulcers and ischemia. Therefore, molecules able to target the VEGF and its receptors are of great pharmaceutical interest. Several types of molecules have been reported so far. In this review, we focus on the structure-based design of peptides mimicking VEGF/VEGFR binding epitopes. The binding interface of the complex has been dissected and the different regions challenged for peptide design. All these trials furnished a better understanding of the molecular recognition process and provide us with a wealth of molecules that could be optimized to be exploited for pharmaceutical applications. |
format | Online Article Text |
id | pubmed-10302803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103028032023-06-29 Structure-Based Design of Peptides Targeting VEGF/VEGFRs Di Stasi, Rossella De Rosa, Lucia D’Andrea, Luca Domenico Pharmaceuticals (Basel) Review Vascular endothelial growth factor (VEGF) and its receptors (VEGFRs) play a main role in the regulation of angiogenesis and lymphangiogenesis. Furthermore, they are implicated in the onset of several diseases such as rheumatoid arthritis, degenerative eye conditions, tumor growth, ulcers and ischemia. Therefore, molecules able to target the VEGF and its receptors are of great pharmaceutical interest. Several types of molecules have been reported so far. In this review, we focus on the structure-based design of peptides mimicking VEGF/VEGFR binding epitopes. The binding interface of the complex has been dissected and the different regions challenged for peptide design. All these trials furnished a better understanding of the molecular recognition process and provide us with a wealth of molecules that could be optimized to be exploited for pharmaceutical applications. MDPI 2023-06-07 /pmc/articles/PMC10302803/ /pubmed/37375798 http://dx.doi.org/10.3390/ph16060851 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 | Review Di Stasi, Rossella De Rosa, Lucia D’Andrea, Luca Domenico Structure-Based Design of Peptides Targeting VEGF/VEGFRs |
title | Structure-Based Design of Peptides Targeting VEGF/VEGFRs |
title_full | Structure-Based Design of Peptides Targeting VEGF/VEGFRs |
title_fullStr | Structure-Based Design of Peptides Targeting VEGF/VEGFRs |
title_full_unstemmed | Structure-Based Design of Peptides Targeting VEGF/VEGFRs |
title_short | Structure-Based Design of Peptides Targeting VEGF/VEGFRs |
title_sort | structure-based design of peptides targeting vegf/vegfrs |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302803/ https://www.ncbi.nlm.nih.gov/pubmed/37375798 http://dx.doi.org/10.3390/ph16060851 |
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