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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...

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Detalles Bibliográficos
Autores principales: Lusvarghi, Sabrina, Bewley, Carole A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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.
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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
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