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TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes

The interaction between the class I major histocompatibility complex (MHC), the peptide presented by the MHC and the T-cell receptor (TCR) is a key determinant of the cellular immune response. Here, we present TCRpMHCmodels, a method for accurate structural modelling of the TCR-peptide-MHC (TCR-pMHC...

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Autores principales: Jensen, Kamilla Kjærgaard, Rantos, Vasileios, Jappe, Emma Christine, Olsen, Tobias Hegelund, Jespersen, Martin Closter, Jurtz, Vanessa, Jessen, Leon Eyrich, Lanzarotti, Esteban, Mahajan, Swapnil, Peters, Bjoern, Nielsen, Morten, Marcatili, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787230/
https://www.ncbi.nlm.nih.gov/pubmed/31601838
http://dx.doi.org/10.1038/s41598-019-50932-4
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author Jensen, Kamilla Kjærgaard
Rantos, Vasileios
Jappe, Emma Christine
Olsen, Tobias Hegelund
Jespersen, Martin Closter
Jurtz, Vanessa
Jessen, Leon Eyrich
Lanzarotti, Esteban
Mahajan, Swapnil
Peters, Bjoern
Nielsen, Morten
Marcatili, Paolo
author_facet Jensen, Kamilla Kjærgaard
Rantos, Vasileios
Jappe, Emma Christine
Olsen, Tobias Hegelund
Jespersen, Martin Closter
Jurtz, Vanessa
Jessen, Leon Eyrich
Lanzarotti, Esteban
Mahajan, Swapnil
Peters, Bjoern
Nielsen, Morten
Marcatili, Paolo
author_sort Jensen, Kamilla Kjærgaard
collection PubMed
description The interaction between the class I major histocompatibility complex (MHC), the peptide presented by the MHC and the T-cell receptor (TCR) is a key determinant of the cellular immune response. Here, we present TCRpMHCmodels, a method for accurate structural modelling of the TCR-peptide-MHC (TCR-pMHC) complex. This TCR-pMHC modelling pipeline takes as input the amino acid sequence and generates models of the TCR-pMHC complex, with a median Cα RMSD of 2.31 Å. TCRpMHCmodels significantly outperforms TCRFlexDock, a specialised method for docking pMHC and TCR structures. TCRpMHCmodels is simple to use and the modelling pipeline takes, on average, only two minutes. Thanks to its ease of use and high modelling accuracy, we expect TCRpMHCmodels to provide insights into the underlying mechanisms of TCR and pMHC interactions and aid in the development of advanced T-cell-based immunotherapies and rational design of vaccines. The TCRpMHCmodels tool is available at http://www.cbs.dtu.dk/services/TCRpMHCmodels/.
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spelling pubmed-67872302019-10-17 TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes Jensen, Kamilla Kjærgaard Rantos, Vasileios Jappe, Emma Christine Olsen, Tobias Hegelund Jespersen, Martin Closter Jurtz, Vanessa Jessen, Leon Eyrich Lanzarotti, Esteban Mahajan, Swapnil Peters, Bjoern Nielsen, Morten Marcatili, Paolo Sci Rep Article The interaction between the class I major histocompatibility complex (MHC), the peptide presented by the MHC and the T-cell receptor (TCR) is a key determinant of the cellular immune response. Here, we present TCRpMHCmodels, a method for accurate structural modelling of the TCR-peptide-MHC (TCR-pMHC) complex. This TCR-pMHC modelling pipeline takes as input the amino acid sequence and generates models of the TCR-pMHC complex, with a median Cα RMSD of 2.31 Å. TCRpMHCmodels significantly outperforms TCRFlexDock, a specialised method for docking pMHC and TCR structures. TCRpMHCmodels is simple to use and the modelling pipeline takes, on average, only two minutes. Thanks to its ease of use and high modelling accuracy, we expect TCRpMHCmodels to provide insights into the underlying mechanisms of TCR and pMHC interactions and aid in the development of advanced T-cell-based immunotherapies and rational design of vaccines. The TCRpMHCmodels tool is available at http://www.cbs.dtu.dk/services/TCRpMHCmodels/. Nature Publishing Group UK 2019-10-10 /pmc/articles/PMC6787230/ /pubmed/31601838 http://dx.doi.org/10.1038/s41598-019-50932-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jensen, Kamilla Kjærgaard
Rantos, Vasileios
Jappe, Emma Christine
Olsen, Tobias Hegelund
Jespersen, Martin Closter
Jurtz, Vanessa
Jessen, Leon Eyrich
Lanzarotti, Esteban
Mahajan, Swapnil
Peters, Bjoern
Nielsen, Morten
Marcatili, Paolo
TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes
title TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes
title_full TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes
title_fullStr TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes
title_full_unstemmed TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes
title_short TCRpMHCmodels: Structural modelling of TCR-pMHC class I complexes
title_sort tcrpmhcmodels: structural modelling of tcr-pmhc class i complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787230/
https://www.ncbi.nlm.nih.gov/pubmed/31601838
http://dx.doi.org/10.1038/s41598-019-50932-4
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