Cargando…

Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development

BACKGROUND: The availability of the P. falciparum genome has led to novel ways to identify potential vaccine candidates. A new approach for antigen discovery based on the bioinformatic selection of heptad repeat motifs corresponding to α-helical coiled coil structures yielded promising results. To e...

Descripción completa

Detalles Bibliográficos
Autores principales: Kulangara, Caroline, Kajava, Andrey V., Corradin, Giampietro, Felger, Ingrid
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683929/
https://www.ncbi.nlm.nih.gov/pubmed/19492090
http://dx.doi.org/10.1371/journal.pone.0005419
_version_ 1782167152776708096
author Kulangara, Caroline
Kajava, Andrey V.
Corradin, Giampietro
Felger, Ingrid
author_facet Kulangara, Caroline
Kajava, Andrey V.
Corradin, Giampietro
Felger, Ingrid
author_sort Kulangara, Caroline
collection PubMed
description BACKGROUND: The availability of the P. falciparum genome has led to novel ways to identify potential vaccine candidates. A new approach for antigen discovery based on the bioinformatic selection of heptad repeat motifs corresponding to α-helical coiled coil structures yielded promising results. To elucidate the question about the relationship between the coiled coil motifs and their sequence conservation, we have assessed the extent of polymorphism in putative α-helical coiled coil domains in culture strains, in natural populations and in the single nucleotide polymorphism data available at PlasmoDB. METHODOLOGY/PRINCIPAL FINDINGS: 14 α-helical coiled coil domains were selected based on preclinical experimental evaluation. They were tested by PCR amplification and sequencing of different P. falciparum culture strains and field isolates. We found that only 3 out of 14 α-helical coiled coils showed point mutations and/or length polymorphisms. Based on promising immunological results 5 of these peptides were selected for further analysis. Direct sequencing of field samples from Papua New Guinea and Tanzania showed that 3 out of these 5 peptides were completely conserved. An in silico analysis of polymorphism was performed for all 166 putative α-helical coiled coil domains originally identified in the P. falciparum genome. We found that 82% (137/166) of these peptides were conserved, and for one peptide only the detected SNPs decreased substantially the probability score for α-helical coiled coil formation. More SNPs were found in arrays of almost perfect tandem repeats. In summary, the coiled coil structure prediction was rarely modified by SNPs. The analysis revealed a number of peptides with strictly conserved α-helical coiled coil motifs. CONCLUSION/SIGNIFICANCE: We conclude that the selection of α-helical coiled coil structural motifs is a valuable approach to identify potential vaccine targets showing a high degree of conservation.
format Text
id pubmed-2683929
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26839292009-06-02 Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development Kulangara, Caroline Kajava, Andrey V. Corradin, Giampietro Felger, Ingrid PLoS One Research Article BACKGROUND: The availability of the P. falciparum genome has led to novel ways to identify potential vaccine candidates. A new approach for antigen discovery based on the bioinformatic selection of heptad repeat motifs corresponding to α-helical coiled coil structures yielded promising results. To elucidate the question about the relationship between the coiled coil motifs and their sequence conservation, we have assessed the extent of polymorphism in putative α-helical coiled coil domains in culture strains, in natural populations and in the single nucleotide polymorphism data available at PlasmoDB. METHODOLOGY/PRINCIPAL FINDINGS: 14 α-helical coiled coil domains were selected based on preclinical experimental evaluation. They were tested by PCR amplification and sequencing of different P. falciparum culture strains and field isolates. We found that only 3 out of 14 α-helical coiled coils showed point mutations and/or length polymorphisms. Based on promising immunological results 5 of these peptides were selected for further analysis. Direct sequencing of field samples from Papua New Guinea and Tanzania showed that 3 out of these 5 peptides were completely conserved. An in silico analysis of polymorphism was performed for all 166 putative α-helical coiled coil domains originally identified in the P. falciparum genome. We found that 82% (137/166) of these peptides were conserved, and for one peptide only the detected SNPs decreased substantially the probability score for α-helical coiled coil formation. More SNPs were found in arrays of almost perfect tandem repeats. In summary, the coiled coil structure prediction was rarely modified by SNPs. The analysis revealed a number of peptides with strictly conserved α-helical coiled coil motifs. CONCLUSION/SIGNIFICANCE: We conclude that the selection of α-helical coiled coil structural motifs is a valuable approach to identify potential vaccine targets showing a high degree of conservation. Public Library of Science 2009-05-25 /pmc/articles/PMC2683929/ /pubmed/19492090 http://dx.doi.org/10.1371/journal.pone.0005419 Text en Kulangara et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kulangara, Caroline
Kajava, Andrey V.
Corradin, Giampietro
Felger, Ingrid
Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development
title Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development
title_full Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development
title_fullStr Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development
title_full_unstemmed Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development
title_short Sequence Conservation in Plasmodium falciparum α-Helical Coiled Coil Domains Proposed for Vaccine Development
title_sort sequence conservation in plasmodium falciparum α-helical coiled coil domains proposed for vaccine development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683929/
https://www.ncbi.nlm.nih.gov/pubmed/19492090
http://dx.doi.org/10.1371/journal.pone.0005419
work_keys_str_mv AT kulangaracaroline sequenceconservationinplasmodiumfalciparumahelicalcoiledcoildomainsproposedforvaccinedevelopment
AT kajavaandreyv sequenceconservationinplasmodiumfalciparumahelicalcoiledcoildomainsproposedforvaccinedevelopment
AT corradingiampietro sequenceconservationinplasmodiumfalciparumahelicalcoiledcoildomainsproposedforvaccinedevelopment
AT felgeringrid sequenceconservationinplasmodiumfalciparumahelicalcoiledcoildomainsproposedforvaccinedevelopment