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Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP
Translationally controlled tumor protein (TCTP), also called histamine releasing factor, is an evolutionarily conserved multifunctional protein in eukaryotes. We previously reported that extracellular TCTP acquires its cytokine-like function following dimerization. This study aims to identify the fu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957494/ https://www.ncbi.nlm.nih.gov/pubmed/31932619 http://dx.doi.org/10.1038/s41598-019-57064-9 |
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author | Lee, Heewon Kim, Mi-Sun Lee, Ji-Sun Cho, Hyunsoo Park, Jimin Hae Shin, Dong Lee, Kyunglim |
author_facet | Lee, Heewon Kim, Mi-Sun Lee, Ji-Sun Cho, Hyunsoo Park, Jimin Hae Shin, Dong Lee, Kyunglim |
author_sort | Lee, Heewon |
collection | PubMed |
description | Translationally controlled tumor protein (TCTP), also called histamine releasing factor, is an evolutionarily conserved multifunctional protein in eukaryotes. We previously reported that extracellular TCTP acquires its cytokine-like function following dimerization. This study aims to identify the functional domain involved in the cytokine-like function of dimerized TCTP (dTCTP). We performed X-ray crystallographic studies and a deletion mutant of dTCTP which lacks the flexible loop domain. Synthetic peptides corresponding to TCTP domains and antibodies developed against them were examined for the anti-allergic effect. In an OVA-induced airway inflammation mouse model, inhibitory effect of synthetic peptides was evaluated. dTCTP was mediated by dimers between Cys172s of TCTP monomers. Synthetic peptides corresponding to the flexible loop and helix 2 domain of TCTP, and antibodies against them inhibited dTCTP-induced IL-8 release. In particular, the TCTP mutant lacking the flexible loop domain decreased the inflammatory cytokine activity of dTCTP. We conclude that the flexible loop and helix 2 domain of TCTP are the functional domains of dTCTP. They may have the potential to be therapeutic targets in the suppression of allergic reactions induced by dTCTP. |
format | Online Article Text |
id | pubmed-6957494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69574942020-01-16 Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP Lee, Heewon Kim, Mi-Sun Lee, Ji-Sun Cho, Hyunsoo Park, Jimin Hae Shin, Dong Lee, Kyunglim Sci Rep Article Translationally controlled tumor protein (TCTP), also called histamine releasing factor, is an evolutionarily conserved multifunctional protein in eukaryotes. We previously reported that extracellular TCTP acquires its cytokine-like function following dimerization. This study aims to identify the functional domain involved in the cytokine-like function of dimerized TCTP (dTCTP). We performed X-ray crystallographic studies and a deletion mutant of dTCTP which lacks the flexible loop domain. Synthetic peptides corresponding to TCTP domains and antibodies developed against them were examined for the anti-allergic effect. In an OVA-induced airway inflammation mouse model, inhibitory effect of synthetic peptides was evaluated. dTCTP was mediated by dimers between Cys172s of TCTP monomers. Synthetic peptides corresponding to the flexible loop and helix 2 domain of TCTP, and antibodies against them inhibited dTCTP-induced IL-8 release. In particular, the TCTP mutant lacking the flexible loop domain decreased the inflammatory cytokine activity of dTCTP. We conclude that the flexible loop and helix 2 domain of TCTP are the functional domains of dTCTP. They may have the potential to be therapeutic targets in the suppression of allergic reactions induced by dTCTP. Nature Publishing Group UK 2020-01-13 /pmc/articles/PMC6957494/ /pubmed/31932619 http://dx.doi.org/10.1038/s41598-019-57064-9 Text en © The Author(s) 2020 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 Lee, Heewon Kim, Mi-Sun Lee, Ji-Sun Cho, Hyunsoo Park, Jimin Hae Shin, Dong Lee, Kyunglim Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP |
title | Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP |
title_full | Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP |
title_fullStr | Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP |
title_full_unstemmed | Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP |
title_short | Flexible loop and helix 2 domains of TCTP are the functional domains of dimerized TCTP |
title_sort | flexible loop and helix 2 domains of tctp are the functional domains of dimerized tctp |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957494/ https://www.ncbi.nlm.nih.gov/pubmed/31932619 http://dx.doi.org/10.1038/s41598-019-57064-9 |
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