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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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/. |
format | Online Article Text |
id | pubmed-6787230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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