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Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents

Programmed ribosomal frameshifting is used by many viruses to regulate the production of structural and enzymatic proteins. Altering the frameshifting efficiencies disrupts the virus life cycle and eliminates or reduces virus production. Ribosomal frameshifting therefore provides a unique target on...

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Detalles Bibliográficos
Autores principales: Dinman, Jonathan D, Ruiz-Echevarria, Maria J, Peltz, Stuart W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd. 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127214/
https://www.ncbi.nlm.nih.gov/pubmed/9586242
http://dx.doi.org/10.1016/S0167-7799(97)01167-0
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author Dinman, Jonathan D
Ruiz-Echevarria, Maria J
Peltz, Stuart W
author_facet Dinman, Jonathan D
Ruiz-Echevarria, Maria J
Peltz, Stuart W
author_sort Dinman, Jonathan D
collection PubMed
description Programmed ribosomal frameshifting is used by many viruses to regulate the production of structural and enzymatic proteins. Altering the frameshifting efficiencies disrupts the virus life cycle and eliminates or reduces virus production. Ribosomal frameshifting therefore provides a unique target on which antiviral agents can function. This article describes a series of rapid assay strategies that have been developed and used to identify potential antiviral agents that target programmed −1 ribosomal frameshifting.
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spelling pubmed-71272142020-04-08 Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents Dinman, Jonathan D Ruiz-Echevarria, Maria J Peltz, Stuart W Trends Biotechnol Article Programmed ribosomal frameshifting is used by many viruses to regulate the production of structural and enzymatic proteins. Altering the frameshifting efficiencies disrupts the virus life cycle and eliminates or reduces virus production. Ribosomal frameshifting therefore provides a unique target on which antiviral agents can function. This article describes a series of rapid assay strategies that have been developed and used to identify potential antiviral agents that target programmed −1 ribosomal frameshifting. Elsevier Science Ltd. 1998-04-01 1999-03-11 /pmc/articles/PMC7127214/ /pubmed/9586242 http://dx.doi.org/10.1016/S0167-7799(97)01167-0 Text en Copyright © 1998 Elsevier Science Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Dinman, Jonathan D
Ruiz-Echevarria, Maria J
Peltz, Stuart W
Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
title Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
title_full Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
title_fullStr Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
title_full_unstemmed Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
title_short Translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
title_sort translating old drugs into new treatments: ribosomal frameshifting as a target for antiviral agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127214/
https://www.ncbi.nlm.nih.gov/pubmed/9586242
http://dx.doi.org/10.1016/S0167-7799(97)01167-0
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