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Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins

BACKGROUND: Current immunological bioinformatic approaches focus on the prediction of allele-specific epitopes capable of triggering immunogenic activity. The prediction of major histocompatibility complex (MHC) class I epitopes is well studied, and various software solutions exist for this purpose....

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Autores principales: Santos, Anderson R, Pereira, Vanessa Bastos, Barbosa, Eudes, Baumbach, Jan, Pauling, Josch, Röttger, Richard, Turk, Meritxell Zurita, Silva, Artur, Miyoshi, Anderson, Azevedo, Vasco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908659/
https://www.ncbi.nlm.nih.gov/pubmed/24564223
http://dx.doi.org/10.1186/1471-2164-14-S6-S4
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author Santos, Anderson R
Pereira, Vanessa Bastos
Barbosa, Eudes
Baumbach, Jan
Pauling, Josch
Röttger, Richard
Turk, Meritxell Zurita
Silva, Artur
Miyoshi, Anderson
Azevedo, Vasco
author_facet Santos, Anderson R
Pereira, Vanessa Bastos
Barbosa, Eudes
Baumbach, Jan
Pauling, Josch
Röttger, Richard
Turk, Meritxell Zurita
Silva, Artur
Miyoshi, Anderson
Azevedo, Vasco
author_sort Santos, Anderson R
collection PubMed
description BACKGROUND: Current immunological bioinformatic approaches focus on the prediction of allele-specific epitopes capable of triggering immunogenic activity. The prediction of major histocompatibility complex (MHC) class I epitopes is well studied, and various software solutions exist for this purpose. However, currently available tools do not account for the concentration of epitope products in the mature protein product and its relation to the reliability of target selection. RESULTS: We developed a computational strategy based on measuring the epitope's concentration in the mature protein, called Mature Epitope Density (MED). Our method, though simple, is capable of identifying promising vaccine targets. Our online software implementation provides a computationally light and reliable analysis of bacterial exoproteins and their potential for vaccines or diagnosis projects against pathogenic organisms. We evaluated our computational approach by using the Mycobacterium tuberculosis (Mtb) H37Rv exoproteome as a gold standard model. A literature search was carried out on 60 out of 553 Mtb's predicted exoproteins, looking for previous experimental evidence concerning their possible antigenicity. Half of the 60 proteins were classified as highest scored by the MED statistic, while the other half were classified as lowest scored. Among the lowest scored proteins, ~13% were confirmed as not related to antigenicity or not contributing to the bacterial pathogenicity, and 70% of the highest scored proteins were confirmed as related. There was no experimental evidence of antigenic or pathogenic contributions for three of the highest MED-scored Mtb proteins. Hence, these three proteins could represent novel putative vaccine and drug targets for Mtb. A web version of MED is publicly available online at http://med.mmci.uni-saarland.de/. CONCLUSIONS: The software presented here offers a practical and accurate method to identify potential vaccine and diagnosis candidates against pathogenic bacteria by "reading" results from well-established reverse vaccinology software in a novel way, considering the epitope's concentration in the mature portion of the protein.
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spelling pubmed-39086592014-02-13 Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins Santos, Anderson R Pereira, Vanessa Bastos Barbosa, Eudes Baumbach, Jan Pauling, Josch Röttger, Richard Turk, Meritxell Zurita Silva, Artur Miyoshi, Anderson Azevedo, Vasco BMC Genomics Research BACKGROUND: Current immunological bioinformatic approaches focus on the prediction of allele-specific epitopes capable of triggering immunogenic activity. The prediction of major histocompatibility complex (MHC) class I epitopes is well studied, and various software solutions exist for this purpose. However, currently available tools do not account for the concentration of epitope products in the mature protein product and its relation to the reliability of target selection. RESULTS: We developed a computational strategy based on measuring the epitope's concentration in the mature protein, called Mature Epitope Density (MED). Our method, though simple, is capable of identifying promising vaccine targets. Our online software implementation provides a computationally light and reliable analysis of bacterial exoproteins and their potential for vaccines or diagnosis projects against pathogenic organisms. We evaluated our computational approach by using the Mycobacterium tuberculosis (Mtb) H37Rv exoproteome as a gold standard model. A literature search was carried out on 60 out of 553 Mtb's predicted exoproteins, looking for previous experimental evidence concerning their possible antigenicity. Half of the 60 proteins were classified as highest scored by the MED statistic, while the other half were classified as lowest scored. Among the lowest scored proteins, ~13% were confirmed as not related to antigenicity or not contributing to the bacterial pathogenicity, and 70% of the highest scored proteins were confirmed as related. There was no experimental evidence of antigenic or pathogenic contributions for three of the highest MED-scored Mtb proteins. Hence, these three proteins could represent novel putative vaccine and drug targets for Mtb. A web version of MED is publicly available online at http://med.mmci.uni-saarland.de/. CONCLUSIONS: The software presented here offers a practical and accurate method to identify potential vaccine and diagnosis candidates against pathogenic bacteria by "reading" results from well-established reverse vaccinology software in a novel way, considering the epitope's concentration in the mature portion of the protein. BioMed Central 2013-10-25 /pmc/articles/PMC3908659/ /pubmed/24564223 http://dx.doi.org/10.1186/1471-2164-14-S6-S4 Text en Copyright © 2013 Santos et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Santos, Anderson R
Pereira, Vanessa Bastos
Barbosa, Eudes
Baumbach, Jan
Pauling, Josch
Röttger, Richard
Turk, Meritxell Zurita
Silva, Artur
Miyoshi, Anderson
Azevedo, Vasco
Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins
title Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins
title_full Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins
title_fullStr Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins
title_full_unstemmed Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins
title_short Mature Epitope Density - A strategy for target selection based on immunoinformatics and exported prokaryotic proteins
title_sort mature epitope density - a strategy for target selection based on immunoinformatics and exported prokaryotic proteins
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908659/
https://www.ncbi.nlm.nih.gov/pubmed/24564223
http://dx.doi.org/10.1186/1471-2164-14-S6-S4
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