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Small Molecules Targeting Viral RNA
The majority of antivirals available target viral proteins; however, RNA is emerging as a new and promising antiviral target due to the presence of highly structured RNA in viral genomes fundamental for their replication cycle. Here, we discuss methods for the identification of RNA-targeting compoun...
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/PMC10487773/ https://www.ncbi.nlm.nih.gov/pubmed/37686306 http://dx.doi.org/10.3390/ijms241713500 |
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author | Mathez, Gregory Cagno, Valeria |
author_facet | Mathez, Gregory Cagno, Valeria |
author_sort | Mathez, Gregory |
collection | PubMed |
description | The majority of antivirals available target viral proteins; however, RNA is emerging as a new and promising antiviral target due to the presence of highly structured RNA in viral genomes fundamental for their replication cycle. Here, we discuss methods for the identification of RNA-targeting compounds, starting from the determination of RNA structures either from purified RNA or in living cells, followed by in silico screening on RNA and phenotypic assays to evaluate viral inhibition. Moreover, we review the small molecules known to target the programmed ribosomal frameshifting element of SARS-CoV-2, the internal ribosomal entry site of different viruses, and RNA elements of HIV. |
format | Online Article Text |
id | pubmed-10487773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104877732023-09-09 Small Molecules Targeting Viral RNA Mathez, Gregory Cagno, Valeria Int J Mol Sci Review The majority of antivirals available target viral proteins; however, RNA is emerging as a new and promising antiviral target due to the presence of highly structured RNA in viral genomes fundamental for their replication cycle. Here, we discuss methods for the identification of RNA-targeting compounds, starting from the determination of RNA structures either from purified RNA or in living cells, followed by in silico screening on RNA and phenotypic assays to evaluate viral inhibition. Moreover, we review the small molecules known to target the programmed ribosomal frameshifting element of SARS-CoV-2, the internal ribosomal entry site of different viruses, and RNA elements of HIV. MDPI 2023-08-31 /pmc/articles/PMC10487773/ /pubmed/37686306 http://dx.doi.org/10.3390/ijms241713500 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 Mathez, Gregory Cagno, Valeria Small Molecules Targeting Viral RNA |
title | Small Molecules Targeting Viral RNA |
title_full | Small Molecules Targeting Viral RNA |
title_fullStr | Small Molecules Targeting Viral RNA |
title_full_unstemmed | Small Molecules Targeting Viral RNA |
title_short | Small Molecules Targeting Viral RNA |
title_sort | small molecules targeting viral rna |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487773/ https://www.ncbi.nlm.nih.gov/pubmed/37686306 http://dx.doi.org/10.3390/ijms241713500 |
work_keys_str_mv | AT mathezgregory smallmoleculestargetingviralrna AT cagnovaleria smallmoleculestargetingviralrna |