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Peptide‐based covalent inhibitors of protein–protein interactions
Protein–protein interactions (PPI) are involved in all cellular processes and many represent attractive therapeutic targets. However, the frequently rather flat and large interaction areas render the identification of small molecular PPI inhibitors very challenging. As an alternative, peptide intera...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077911/ https://www.ncbi.nlm.nih.gov/pubmed/36239115 http://dx.doi.org/10.1002/psc.3457 |
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author | Paulussen, Felix M. Grossmann, Tom N. |
author_facet | Paulussen, Felix M. Grossmann, Tom N. |
author_sort | Paulussen, Felix M. |
collection | PubMed |
description | Protein–protein interactions (PPI) are involved in all cellular processes and many represent attractive therapeutic targets. However, the frequently rather flat and large interaction areas render the identification of small molecular PPI inhibitors very challenging. As an alternative, peptide interaction motifs derived from a PPI interface can serve as starting points for the development of inhibitors. However, certain proteins remain challenging targets when applying inhibitors with a competitive mode of action. For that reason, peptide‐based ligands with an irreversible binding mode have gained attention in recent years. This review summarizes examples of covalent inhibitors that employ peptidic binders and have been tested in a biological context. |
format | Online Article Text |
id | pubmed-10077911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100779112023-04-07 Peptide‐based covalent inhibitors of protein–protein interactions Paulussen, Felix M. Grossmann, Tom N. J Pept Sci Review Protein–protein interactions (PPI) are involved in all cellular processes and many represent attractive therapeutic targets. However, the frequently rather flat and large interaction areas render the identification of small molecular PPI inhibitors very challenging. As an alternative, peptide interaction motifs derived from a PPI interface can serve as starting points for the development of inhibitors. However, certain proteins remain challenging targets when applying inhibitors with a competitive mode of action. For that reason, peptide‐based ligands with an irreversible binding mode have gained attention in recent years. This review summarizes examples of covalent inhibitors that employ peptidic binders and have been tested in a biological context. John Wiley and Sons Inc. 2022-11-09 2023-01 /pmc/articles/PMC10077911/ /pubmed/36239115 http://dx.doi.org/10.1002/psc.3457 Text en © 2022 The Authors. Journal of Peptide Science published by European Peptide Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Paulussen, Felix M. Grossmann, Tom N. Peptide‐based covalent inhibitors of protein–protein interactions |
title | Peptide‐based covalent inhibitors of protein–protein interactions |
title_full | Peptide‐based covalent inhibitors of protein–protein interactions |
title_fullStr | Peptide‐based covalent inhibitors of protein–protein interactions |
title_full_unstemmed | Peptide‐based covalent inhibitors of protein–protein interactions |
title_short | Peptide‐based covalent inhibitors of protein–protein interactions |
title_sort | peptide‐based covalent inhibitors of protein–protein interactions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077911/ https://www.ncbi.nlm.nih.gov/pubmed/36239115 http://dx.doi.org/10.1002/psc.3457 |
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