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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/17954
Ver los metadatos del registro completo
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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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1842269619853721600 |
score |
13.13397 |