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Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers

Influenza A virus subtype H5N1 is highly contagious among birds, causing high mortality among domestic poultry. The viral genome is contained on eight single RNA strands of which HA encode the antigenic glycoprotein called hemagglutinin. Hemagglutinin found on the surface of the influenza viruses an...

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Detalles Bibliográficos
Autores principales: Dhar, Ganguli, Sayak, Datta, Abhijit
Formato: Texto
Lenguaje:English
Publicado: Biomedical Informatics Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2859575/
https://www.ncbi.nlm.nih.gov/pubmed/20461158
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author Dhar,
Ganguli, Sayak
Datta, Abhijit
author_facet Dhar,
Ganguli, Sayak
Datta, Abhijit
author_sort Dhar,
collection PubMed
description Influenza A virus subtype H5N1 is highly contagious among birds, causing high mortality among domestic poultry. The viral genome is contained on eight single RNA strands of which HA encode the antigenic glycoprotein called hemagglutinin. Hemagglutinin found on the surface of the influenza viruses and is responsible for binding the virus to the cell that is being infected. Among the most prevalent RNA structures the pseudoknot motif represents an important piece of RNA architecture, as it provides a means for a single RNA strand to fold upon itself to produce a globular structure capable of performing important biological functions. In this analysis we have identified the pseudoknot motifs in the hemagglutinin gene of HPAI A (H5N1) Asian strains. Specific aptamers have been designed against these pseudoknots. These in-silico aptamers can be used to hinder the ability of pseudoknots to facilitate ribosomal frameshifting. This may ultimately lead to reduce the coding efficiency of the HA that encodes hemagglutinin and might be used as molecular medicine for H5N1.
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spelling pubmed-28595752010-05-11 Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers Dhar, Ganguli, Sayak Datta, Abhijit Bioinformation Hypothesis Influenza A virus subtype H5N1 is highly contagious among birds, causing high mortality among domestic poultry. The viral genome is contained on eight single RNA strands of which HA encode the antigenic glycoprotein called hemagglutinin. Hemagglutinin found on the surface of the influenza viruses and is responsible for binding the virus to the cell that is being infected. Among the most prevalent RNA structures the pseudoknot motif represents an important piece of RNA architecture, as it provides a means for a single RNA strand to fold upon itself to produce a globular structure capable of performing important biological functions. In this analysis we have identified the pseudoknot motifs in the hemagglutinin gene of HPAI A (H5N1) Asian strains. Specific aptamers have been designed against these pseudoknots. These in-silico aptamers can be used to hinder the ability of pseudoknots to facilitate ribosomal frameshifting. This may ultimately lead to reduce the coding efficiency of the HA that encodes hemagglutinin and might be used as molecular medicine for H5N1. Biomedical Informatics Publishing Group 2009-10-25 /pmc/articles/PMC2859575/ /pubmed/20461158 Text en © 2009 Biomedical Informatics Publishing Group This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Dhar,
Ganguli, Sayak
Datta, Abhijit
Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers
title Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers
title_full Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers
title_fullStr Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers
title_full_unstemmed Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers
title_short Targeting pseudoknots in H5N1 hemagglutinin using designed aptamers
title_sort targeting pseudoknots in h5n1 hemagglutinin using designed aptamers
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2859575/
https://www.ncbi.nlm.nih.gov/pubmed/20461158
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