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RNA-Binding Macrocyclic Peptides

Being able to effectively target RNA with potent ligands will open up a large number of potential therapeutic options. The knowledge on how to achieve this is ever expanding but an important question that remains open is what chemical matter is suitable to achieve this goal. The high flexibility of...

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Detalles Bibliográficos
Autores principales: Pal, Sunit, ‘t Hart, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062085/
https://www.ncbi.nlm.nih.gov/pubmed/35517859
http://dx.doi.org/10.3389/fmolb.2022.883060
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author Pal, Sunit
‘t Hart, Peter
author_facet Pal, Sunit
‘t Hart, Peter
author_sort Pal, Sunit
collection PubMed
description Being able to effectively target RNA with potent ligands will open up a large number of potential therapeutic options. The knowledge on how to achieve this is ever expanding but an important question that remains open is what chemical matter is suitable to achieve this goal. The high flexibility of an RNA as well as its more limited chemical diversity and featureless binding sites can be difficult to target selectively but can be addressed by well-designed cyclic peptides. In this review we will provide an overview of reported cyclic peptide ligands for therapeutically relevant RNA targets and discuss the methods used to discover them. We will also provide critical insights into the properties required for potent and selective interaction and suggestions on how to assess these parameters. The use of cyclic peptides to target RNA is still in its infancy but the lessons learned from past examples can be adopted for the development of novel potent and selective ligands.
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spelling pubmed-90620852022-05-04 RNA-Binding Macrocyclic Peptides Pal, Sunit ‘t Hart, Peter Front Mol Biosci Molecular Biosciences Being able to effectively target RNA with potent ligands will open up a large number of potential therapeutic options. The knowledge on how to achieve this is ever expanding but an important question that remains open is what chemical matter is suitable to achieve this goal. The high flexibility of an RNA as well as its more limited chemical diversity and featureless binding sites can be difficult to target selectively but can be addressed by well-designed cyclic peptides. In this review we will provide an overview of reported cyclic peptide ligands for therapeutically relevant RNA targets and discuss the methods used to discover them. We will also provide critical insights into the properties required for potent and selective interaction and suggestions on how to assess these parameters. The use of cyclic peptides to target RNA is still in its infancy but the lessons learned from past examples can be adopted for the development of novel potent and selective ligands. Frontiers Media S.A. 2022-04-19 /pmc/articles/PMC9062085/ /pubmed/35517859 http://dx.doi.org/10.3389/fmolb.2022.883060 Text en Copyright © 2022 Pal and ‘t Hart. 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 Molecular Biosciences
Pal, Sunit
‘t Hart, Peter
RNA-Binding Macrocyclic Peptides
title RNA-Binding Macrocyclic Peptides
title_full RNA-Binding Macrocyclic Peptides
title_fullStr RNA-Binding Macrocyclic Peptides
title_full_unstemmed RNA-Binding Macrocyclic Peptides
title_short RNA-Binding Macrocyclic Peptides
title_sort rna-binding macrocyclic peptides
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062085/
https://www.ncbi.nlm.nih.gov/pubmed/35517859
http://dx.doi.org/10.3389/fmolb.2022.883060
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