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Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential
Griffithsin (GRFT), an algae-derived lectin, is one of the most potent viral entry inhibitors discovered to date. It is currently being developed as a microbicide with broad-spectrum activity against several enveloped viruses. GRFT can inhibit human immunodeficiency virus (HIV) infection at picomola...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086628/ https://www.ncbi.nlm.nih.gov/pubmed/27783038 http://dx.doi.org/10.3390/v8100296 |
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author | Lusvarghi, Sabrina Bewley, Carole A. |
author_facet | Lusvarghi, Sabrina Bewley, Carole A. |
author_sort | Lusvarghi, Sabrina |
collection | PubMed |
description | Griffithsin (GRFT), an algae-derived lectin, is one of the most potent viral entry inhibitors discovered to date. It is currently being developed as a microbicide with broad-spectrum activity against several enveloped viruses. GRFT can inhibit human immunodeficiency virus (HIV) infection at picomolar concentrations, surpassing the ability of most anti-HIV agents. The potential to inhibit other viruses as well as parasites has also been demonstrated. Griffithsin’s antiviral activity stems from its ability to bind terminal mannoses present in high-mannose oligosaccharides and crosslink these glycans on the surface of the viral envelope glycoproteins. Here, we review structural and biochemical studies that established mode of action and facilitated construction of GRFT analogs, mechanisms that may lead to resistance, and in vitro and pre-clinical results that support the therapeutic potential of this lectin. |
format | Online Article Text |
id | pubmed-5086628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50866282016-11-02 Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential Lusvarghi, Sabrina Bewley, Carole A. Viruses Review Griffithsin (GRFT), an algae-derived lectin, is one of the most potent viral entry inhibitors discovered to date. It is currently being developed as a microbicide with broad-spectrum activity against several enveloped viruses. GRFT can inhibit human immunodeficiency virus (HIV) infection at picomolar concentrations, surpassing the ability of most anti-HIV agents. The potential to inhibit other viruses as well as parasites has also been demonstrated. Griffithsin’s antiviral activity stems from its ability to bind terminal mannoses present in high-mannose oligosaccharides and crosslink these glycans on the surface of the viral envelope glycoproteins. Here, we review structural and biochemical studies that established mode of action and facilitated construction of GRFT analogs, mechanisms that may lead to resistance, and in vitro and pre-clinical results that support the therapeutic potential of this lectin. MDPI 2016-10-24 /pmc/articles/PMC5086628/ /pubmed/27783038 http://dx.doi.org/10.3390/v8100296 Text en © 2016 by the authors; 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 Lusvarghi, Sabrina Bewley, Carole A. Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential |
title | Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential |
title_full | Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential |
title_fullStr | Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential |
title_full_unstemmed | Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential |
title_short | Griffithsin: An Antiviral Lectin with Outstanding Therapeutic Potential |
title_sort | griffithsin: an antiviral lectin with outstanding therapeutic potential |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086628/ https://www.ncbi.nlm.nih.gov/pubmed/27783038 http://dx.doi.org/10.3390/v8100296 |
work_keys_str_mv | AT lusvarghisabrina griffithsinanantivirallectinwithoutstandingtherapeuticpotential AT bewleycarolea griffithsinanantivirallectinwithoutstandingtherapeuticpotential |