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TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs
MOTIVATION: T cells use T cell receptors (TCRs) to recognize small parts of antigens, called epitopes, presented by major histocompatibility complexes. Once an epitope is recognized, an immune response is initiated and T cell activation and proliferation by clonal expansion begin. Clonal populations...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825763/ https://www.ncbi.nlm.nih.gov/pubmed/36477794 http://dx.doi.org/10.1093/bioinformatics/btac788 |
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author | Jokinen, Emmi Dumitrescu, Alexandru Huuhtanen, Jani Gligorijević, Vladimir Mustjoki, Satu Bonneau, Richard Heinonen, Markus Lähdesmäki, Harri |
author_facet | Jokinen, Emmi Dumitrescu, Alexandru Huuhtanen, Jani Gligorijević, Vladimir Mustjoki, Satu Bonneau, Richard Heinonen, Markus Lähdesmäki, Harri |
author_sort | Jokinen, Emmi |
collection | PubMed |
description | MOTIVATION: T cells use T cell receptors (TCRs) to recognize small parts of antigens, called epitopes, presented by major histocompatibility complexes. Once an epitope is recognized, an immune response is initiated and T cell activation and proliferation by clonal expansion begin. Clonal populations of T cells with identical TCRs can remain in the body for years, thus forming immunological memory and potentially mappable immunological signatures, which could have implications in clinical applications including infectious diseases, autoimmunity and tumor immunology. RESULTS: We introduce TCRconv, a deep learning model for predicting recognition between TCRs and epitopes. TCRconv uses a deep protein language model and convolutions to extract contextualized motifs and provides state-of-the-art TCR-epitope prediction accuracy. Using TCR repertoires from COVID-19 patients, we demonstrate that TCRconv can provide insight into T cell dynamics and phenotypes during the disease. AVAILABILITY AND IMPLEMENTATION: TCRconv is available at https://github.com/emmijokinen/tcrconv. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-9825763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98257632023-01-10 TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs Jokinen, Emmi Dumitrescu, Alexandru Huuhtanen, Jani Gligorijević, Vladimir Mustjoki, Satu Bonneau, Richard Heinonen, Markus Lähdesmäki, Harri Bioinformatics Original Paper MOTIVATION: T cells use T cell receptors (TCRs) to recognize small parts of antigens, called epitopes, presented by major histocompatibility complexes. Once an epitope is recognized, an immune response is initiated and T cell activation and proliferation by clonal expansion begin. Clonal populations of T cells with identical TCRs can remain in the body for years, thus forming immunological memory and potentially mappable immunological signatures, which could have implications in clinical applications including infectious diseases, autoimmunity and tumor immunology. RESULTS: We introduce TCRconv, a deep learning model for predicting recognition between TCRs and epitopes. TCRconv uses a deep protein language model and convolutions to extract contextualized motifs and provides state-of-the-art TCR-epitope prediction accuracy. Using TCR repertoires from COVID-19 patients, we demonstrate that TCRconv can provide insight into T cell dynamics and phenotypes during the disease. AVAILABILITY AND IMPLEMENTATION: TCRconv is available at https://github.com/emmijokinen/tcrconv. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-12-07 /pmc/articles/PMC9825763/ /pubmed/36477794 http://dx.doi.org/10.1093/bioinformatics/btac788 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Jokinen, Emmi Dumitrescu, Alexandru Huuhtanen, Jani Gligorijević, Vladimir Mustjoki, Satu Bonneau, Richard Heinonen, Markus Lähdesmäki, Harri TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs |
title | TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs |
title_full | TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs |
title_fullStr | TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs |
title_full_unstemmed | TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs |
title_short | TCRconv: predicting recognition between T cell receptors and epitopes using contextualized motifs |
title_sort | tcrconv: predicting recognition between t cell receptors and epitopes using contextualized motifs |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825763/ https://www.ncbi.nlm.nih.gov/pubmed/36477794 http://dx.doi.org/10.1093/bioinformatics/btac788 |
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