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Mapping, Structure and Modulation of PPI
Because of the key relevance of protein–protein interactions (PPI) in diseases, the modulation of protein-protein complexes is of relevant clinical significance. The successful design of binding compounds modulating PPI requires a detailed knowledge of the involved protein-protein system at molecula...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529325/ https://www.ncbi.nlm.nih.gov/pubmed/34692637 http://dx.doi.org/10.3389/fchem.2021.718405 |
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author | Martino, Elisa Chiarugi, Sara Margheriti, Francesco Garau, Gianpiero |
author_facet | Martino, Elisa Chiarugi, Sara Margheriti, Francesco Garau, Gianpiero |
author_sort | Martino, Elisa |
collection | PubMed |
description | Because of the key relevance of protein–protein interactions (PPI) in diseases, the modulation of protein-protein complexes is of relevant clinical significance. The successful design of binding compounds modulating PPI requires a detailed knowledge of the involved protein-protein system at molecular level, and investigation of the structural motifs that drive the association of the proteins at the recognition interface. These elements represent hot spots of the protein binding free energy, define the complex lifetime and possible modulation strategies. Here, we review the advanced technologies used to map the PPI involved in human diseases, to investigate the structure-function features of protein complexes, and to discover effective ligands that modulate the PPI for therapeutic intervention. |
format | Online Article Text |
id | pubmed-8529325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85293252021-10-22 Mapping, Structure and Modulation of PPI Martino, Elisa Chiarugi, Sara Margheriti, Francesco Garau, Gianpiero Front Chem Chemistry Because of the key relevance of protein–protein interactions (PPI) in diseases, the modulation of protein-protein complexes is of relevant clinical significance. The successful design of binding compounds modulating PPI requires a detailed knowledge of the involved protein-protein system at molecular level, and investigation of the structural motifs that drive the association of the proteins at the recognition interface. These elements represent hot spots of the protein binding free energy, define the complex lifetime and possible modulation strategies. Here, we review the advanced technologies used to map the PPI involved in human diseases, to investigate the structure-function features of protein complexes, and to discover effective ligands that modulate the PPI for therapeutic intervention. Frontiers Media S.A. 2021-10-07 /pmc/articles/PMC8529325/ /pubmed/34692637 http://dx.doi.org/10.3389/fchem.2021.718405 Text en Copyright © 2021 Martino, Chiarugi, Margheriti and Garau. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Martino, Elisa Chiarugi, Sara Margheriti, Francesco Garau, Gianpiero Mapping, Structure and Modulation of PPI |
title | Mapping, Structure and Modulation of PPI |
title_full | Mapping, Structure and Modulation of PPI |
title_fullStr | Mapping, Structure and Modulation of PPI |
title_full_unstemmed | Mapping, Structure and Modulation of PPI |
title_short | Mapping, Structure and Modulation of PPI |
title_sort | mapping, structure and modulation of ppi |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529325/ https://www.ncbi.nlm.nih.gov/pubmed/34692637 http://dx.doi.org/10.3389/fchem.2021.718405 |
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