Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment

Autores
Carrasco Pro, Sebastián; Zimic, Mirko; Nielsen, Morten
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Major histocompatibility complex (MHC) molecules play a key role in cell-mediated immune responses presenting bounded peptides for recognition by the immune system cells. Several in silico methods have been developed to predict the binding affinity of a given peptide to a specific MHC molecule. One of the current state-of-the-art methods for MHC class I is NetMHCpan, which has a core ingredient for the representation of the MHC class I molecule using a pseudo-sequence representation of the binding cleft amino acid environment. New and large MHC–peptide-binding data sets are constantly being made available, and also new structures of MHC class I molecules with a bound peptide have been published. In order to test if the NetMHCpan method can be improved by integrating this novel information, we created new pseudo-sequence definitions for the MHC-binding cleft environment from sequence and structural analyses of different MHC data sets including human leukocyte antigen (HLA), non-human primates (chimpanzee, macaque and gorilla) and other animal alleles (cattle, mouse and swine). From these constructs, we showed that by focusing on MHC sequence positions found to be polymorphic across the MHC molecules used to train the method, the NetMHCpan method achieved a significant increase in the predictive performance, in particular, of non-human MHCs. This study hence showed that an improved performance of MHC-binding methods can be achieved not only by the accumulation of more MHC–peptide-binding data but also by a refined definition of the MHC-binding environment including information from non-human species.
Fil: Carrasco Pro, Sebastián. Universidad Peruana Cayetano Heredia; Perú
Fil: Zimic, Mirko. Universidad Peruana Cayetano Heredia; Perú
Fil: Nielsen, Morten. Technical University of Denmark; Dinamarca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentina
Materia
MHC
peptide binding
Specificity
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/17954

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network_name_str CONICET Digital (CONICET)
spelling Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environmentCarrasco Pro, SebastiánZimic, MirkoNielsen, MortenMHCpeptide bindingSpecificityhttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Major histocompatibility complex (MHC) molecules play a key role in cell-mediated immune responses presenting bounded peptides for recognition by the immune system cells. Several in silico methods have been developed to predict the binding affinity of a given peptide to a specific MHC molecule. One of the current state-of-the-art methods for MHC class I is NetMHCpan, which has a core ingredient for the representation of the MHC class I molecule using a pseudo-sequence representation of the binding cleft amino acid environment. New and large MHC–peptide-binding data sets are constantly being made available, and also new structures of MHC class I molecules with a bound peptide have been published. In order to test if the NetMHCpan method can be improved by integrating this novel information, we created new pseudo-sequence definitions for the MHC-binding cleft environment from sequence and structural analyses of different MHC data sets including human leukocyte antigen (HLA), non-human primates (chimpanzee, macaque and gorilla) and other animal alleles (cattle, mouse and swine). From these constructs, we showed that by focusing on MHC sequence positions found to be polymorphic across the MHC molecules used to train the method, the NetMHCpan method achieved a significant increase in the predictive performance, in particular, of non-human MHCs. This study hence showed that an improved performance of MHC-binding methods can be achieved not only by the accumulation of more MHC–peptide-binding data but also by a refined definition of the MHC-binding environment including information from non-human species.Fil: Carrasco Pro, Sebastián. Universidad Peruana Cayetano Heredia; PerúFil: Zimic, Mirko. Universidad Peruana Cayetano Heredia; PerúFil: Nielsen, Morten. Technical University of Denmark; Dinamarca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; ArgentinaWiley2014-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/17954Carrasco Pro, Sebastián; Zimic, Mirko; Nielsen, Morten; Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment; Wiley; Tissue Antigens; 83; 2; 2-2014; 94-1000001-28152059-2310enginfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1111/tan.12292/abstractinfo:eu-repo/semantics/altIdentifier/doi/10.1111/tan.12292info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925504/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:00:06Zoai:ri.conicet.gov.ar:11336/17954instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:00:06.649CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
title Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
spellingShingle Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
Carrasco Pro, Sebastián
MHC
peptide binding
Specificity
title_short Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
title_full Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
title_fullStr Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
title_full_unstemmed Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
title_sort Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment
dc.creator.none.fl_str_mv Carrasco Pro, Sebastián
Zimic, Mirko
Nielsen, Morten
author Carrasco Pro, Sebastián
author_facet Carrasco Pro, Sebastián
Zimic, Mirko
Nielsen, Morten
author_role author
author2 Zimic, Mirko
Nielsen, Morten
author2_role author
author
dc.subject.none.fl_str_mv MHC
peptide binding
Specificity
topic MHC
peptide binding
Specificity
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Major histocompatibility complex (MHC) molecules play a key role in cell-mediated immune responses presenting bounded peptides for recognition by the immune system cells. Several in silico methods have been developed to predict the binding affinity of a given peptide to a specific MHC molecule. One of the current state-of-the-art methods for MHC class I is NetMHCpan, which has a core ingredient for the representation of the MHC class I molecule using a pseudo-sequence representation of the binding cleft amino acid environment. New and large MHC–peptide-binding data sets are constantly being made available, and also new structures of MHC class I molecules with a bound peptide have been published. In order to test if the NetMHCpan method can be improved by integrating this novel information, we created new pseudo-sequence definitions for the MHC-binding cleft environment from sequence and structural analyses of different MHC data sets including human leukocyte antigen (HLA), non-human primates (chimpanzee, macaque and gorilla) and other animal alleles (cattle, mouse and swine). From these constructs, we showed that by focusing on MHC sequence positions found to be polymorphic across the MHC molecules used to train the method, the NetMHCpan method achieved a significant increase in the predictive performance, in particular, of non-human MHCs. This study hence showed that an improved performance of MHC-binding methods can be achieved not only by the accumulation of more MHC–peptide-binding data but also by a refined definition of the MHC-binding environment including information from non-human species.
Fil: Carrasco Pro, Sebastián. Universidad Peruana Cayetano Heredia; Perú
Fil: Zimic, Mirko. Universidad Peruana Cayetano Heredia; Perú
Fil: Nielsen, Morten. Technical University of Denmark; Dinamarca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentina
description Major histocompatibility complex (MHC) molecules play a key role in cell-mediated immune responses presenting bounded peptides for recognition by the immune system cells. Several in silico methods have been developed to predict the binding affinity of a given peptide to a specific MHC molecule. One of the current state-of-the-art methods for MHC class I is NetMHCpan, which has a core ingredient for the representation of the MHC class I molecule using a pseudo-sequence representation of the binding cleft amino acid environment. New and large MHC–peptide-binding data sets are constantly being made available, and also new structures of MHC class I molecules with a bound peptide have been published. In order to test if the NetMHCpan method can be improved by integrating this novel information, we created new pseudo-sequence definitions for the MHC-binding cleft environment from sequence and structural analyses of different MHC data sets including human leukocyte antigen (HLA), non-human primates (chimpanzee, macaque and gorilla) and other animal alleles (cattle, mouse and swine). From these constructs, we showed that by focusing on MHC sequence positions found to be polymorphic across the MHC molecules used to train the method, the NetMHCpan method achieved a significant increase in the predictive performance, in particular, of non-human MHCs. This study hence showed that an improved performance of MHC-binding methods can be achieved not only by the accumulation of more MHC–peptide-binding data but also by a refined definition of the MHC-binding environment including information from non-human species.
publishDate 2014
dc.date.none.fl_str_mv 2014-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/17954
Carrasco Pro, Sebastián; Zimic, Mirko; Nielsen, Morten; Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment; Wiley; Tissue Antigens; 83; 2; 2-2014; 94-100
0001-2815
2059-2310
url http://hdl.handle.net/11336/17954
identifier_str_mv Carrasco Pro, Sebastián; Zimic, Mirko; Nielsen, Morten; Improved pan-specific MHC class I peptide binding predictions using a novel representation of the MHC binding cleft environment; Wiley; Tissue Antigens; 83; 2; 2-2014; 94-100
0001-2815
2059-2310
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1111/tan.12292/abstract
info:eu-repo/semantics/altIdentifier/doi/10.1111/tan.12292
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925504/
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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