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The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases

A wide variety of viruses exploit furin and other proprotein convertases (PCs) of the constitutive protein secretion pathway in order to regulate their cell entry mechanism and infectivity. Surface proteins of enveloped, as well as non-enveloped, viruses become processed by these proteases intracell...

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Detalles Bibliográficos
Autor principal: Izaguirre, Gonzalo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784293/
https://www.ncbi.nlm.nih.gov/pubmed/31505793
http://dx.doi.org/10.3390/v11090837
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author Izaguirre, Gonzalo
author_facet Izaguirre, Gonzalo
author_sort Izaguirre, Gonzalo
collection PubMed
description A wide variety of viruses exploit furin and other proprotein convertases (PCs) of the constitutive protein secretion pathway in order to regulate their cell entry mechanism and infectivity. Surface proteins of enveloped, as well as non-enveloped, viruses become processed by these proteases intracellularly during morphogenesis or extracellularly after egress and during entry in order to produce mature virions activated for infection. Although viruses also take advantage of other proteases, it is when some viruses become reactive with PCs that they may develop high pathogenicity. Besides reacting with furin, some viruses may also react with the PCs of the other specificity group constituted by PC4/PC5/PACE4/PC7. The targeting of PCs for inhibition may result in a useful strategy to treat infections with some highly pathogenic viruses. A wide variety of PC inhibitors have been developed and tested for their antiviral activity in cell-based assays.
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spelling pubmed-67842932019-10-16 The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases Izaguirre, Gonzalo Viruses Review A wide variety of viruses exploit furin and other proprotein convertases (PCs) of the constitutive protein secretion pathway in order to regulate their cell entry mechanism and infectivity. Surface proteins of enveloped, as well as non-enveloped, viruses become processed by these proteases intracellularly during morphogenesis or extracellularly after egress and during entry in order to produce mature virions activated for infection. Although viruses also take advantage of other proteases, it is when some viruses become reactive with PCs that they may develop high pathogenicity. Besides reacting with furin, some viruses may also react with the PCs of the other specificity group constituted by PC4/PC5/PACE4/PC7. The targeting of PCs for inhibition may result in a useful strategy to treat infections with some highly pathogenic viruses. A wide variety of PC inhibitors have been developed and tested for their antiviral activity in cell-based assays. MDPI 2019-09-09 /pmc/articles/PMC6784293/ /pubmed/31505793 http://dx.doi.org/10.3390/v11090837 Text en © 2019 by the author. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Izaguirre, Gonzalo
The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases
title The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases
title_full The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases
title_fullStr The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases
title_full_unstemmed The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases
title_short The Proteolytic Regulation of Virus Cell Entry by Furin and Other Proprotein Convertases
title_sort proteolytic regulation of virus cell entry by furin and other proprotein convertases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784293/
https://www.ncbi.nlm.nih.gov/pubmed/31505793
http://dx.doi.org/10.3390/v11090837
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