Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin

<p>Abstract</p> <p>Background</p> <p>Hepatitis C Virus (HCV) has two envelop proteins E1 and E2 which is highly glycosylated and play an important role in cell entry. Inhibition of virus at entry step is an important target to find antiviral drugs against HCV. Glanthus...

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Main Authors: Nawaz Zafar, Khaliq Saba, Masoud Muhammad S, Ashfaq Usman A, Riazuddin Sheikh
Format: Article
Language:English
Published: BMC 2011-05-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/8/1/248
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spelling doaj-4dbfae09cf6b41b6974066d3a711792d2020-11-25T00:37:43ZengBMCVirology Journal1743-422X2011-05-018124810.1186/1743-422X-8-248Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis AgglutininNawaz ZafarKhaliq SabaMasoud Muhammad SAshfaq Usman ARiazuddin Sheikh<p>Abstract</p> <p>Background</p> <p>Hepatitis C Virus (HCV) has two envelop proteins E1 and E2 which is highly glycosylated and play an important role in cell entry. Inhibition of virus at entry step is an important target to find antiviral drugs against HCV. Glanthus Nivalis Agglutinin (GNA) is a mannose binding lectin which has tendency for specific recognition and reversible binding to the sugar moieties of a wide variety of glycoproteins of enveloped viruses.</p> <p>Results</p> <p>In the present study, HCV pseudoparticles (HCVpp) for genotype 3a were produced to investigate the ability of GNA to block the HCV entry. The results demonstrated that GNA inhibit the infectivity of HCVpp and HCV infected serum in a dose-dependent manner and resulted in 50% reduction of virus at 1 ± 2 μg concentration. Molecular docking of GNA and HCV glycoproteins (E1 and E2) showed that GNA inhibit HCV entry by binding N-linked glycans.</p> <p>Conclusion</p> <p>These results demonstrated that targeting the HCV glycans is a new approach to develop antiviral drugs against HCV.</p> http://www.virologyj.com/content/8/1/248
collection DOAJ
language English
format Article
sources DOAJ
author Nawaz Zafar
Khaliq Saba
Masoud Muhammad S
Ashfaq Usman A
Riazuddin Sheikh
spellingShingle Nawaz Zafar
Khaliq Saba
Masoud Muhammad S
Ashfaq Usman A
Riazuddin Sheikh
Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin
Virology Journal
author_facet Nawaz Zafar
Khaliq Saba
Masoud Muhammad S
Ashfaq Usman A
Riazuddin Sheikh
author_sort Nawaz Zafar
title Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin
title_short Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin
title_full Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin
title_fullStr Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin
title_full_unstemmed Inhibition of Hepatitis C Virus 3a genotype entry through Glanthus Nivalis Agglutinin
title_sort inhibition of hepatitis c virus 3a genotype entry through glanthus nivalis agglutinin
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2011-05-01
description <p>Abstract</p> <p>Background</p> <p>Hepatitis C Virus (HCV) has two envelop proteins E1 and E2 which is highly glycosylated and play an important role in cell entry. Inhibition of virus at entry step is an important target to find antiviral drugs against HCV. Glanthus Nivalis Agglutinin (GNA) is a mannose binding lectin which has tendency for specific recognition and reversible binding to the sugar moieties of a wide variety of glycoproteins of enveloped viruses.</p> <p>Results</p> <p>In the present study, HCV pseudoparticles (HCVpp) for genotype 3a were produced to investigate the ability of GNA to block the HCV entry. The results demonstrated that GNA inhibit the infectivity of HCVpp and HCV infected serum in a dose-dependent manner and resulted in 50% reduction of virus at 1 ± 2 μg concentration. Molecular docking of GNA and HCV glycoproteins (E1 and E2) showed that GNA inhibit HCV entry by binding N-linked glycans.</p> <p>Conclusion</p> <p>These results demonstrated that targeting the HCV glycans is a new approach to develop antiviral drugs against HCV.</p>
url http://www.virologyj.com/content/8/1/248
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