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Protein-protein-interaction Network Organization of the Hypusine Modification System
Hypusine modification of eukaryotic initiation factor 5A (eIF-5A) represents a unique and highly specific post-translational modification with regulatory functions in cancer, diabetes, and infectious diseases. However, the specific cellular pathways that are influenced by the hypusine modification r...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Biochemistry and Molecular Biology
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494187/ https://www.ncbi.nlm.nih.gov/pubmed/22888148 http://dx.doi.org/10.1074/mcp.M112.019059 |
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author | Sievert, Henning Venz, Simone Platas-Barradas, Oscar Dhople, Vishnu M. Schaletzky, Martin Nagel, Claus-Henning Braig, Melanie Preukschas, Michael Pällmann, Nora Bokemeyer, Carsten Brümmendorf, Tim H. Pörtner, Ralf Walther, Reinhard Duncan, Kent E. Hauber, Joachim Balabanov, Stefan |
author_facet | Sievert, Henning Venz, Simone Platas-Barradas, Oscar Dhople, Vishnu M. Schaletzky, Martin Nagel, Claus-Henning Braig, Melanie Preukschas, Michael Pällmann, Nora Bokemeyer, Carsten Brümmendorf, Tim H. Pörtner, Ralf Walther, Reinhard Duncan, Kent E. Hauber, Joachim Balabanov, Stefan |
author_sort | Sievert, Henning |
collection | PubMed |
description | Hypusine modification of eukaryotic initiation factor 5A (eIF-5A) represents a unique and highly specific post-translational modification with regulatory functions in cancer, diabetes, and infectious diseases. However, the specific cellular pathways that are influenced by the hypusine modification remain largely unknown. To globally characterize eIF-5A and hypusine-dependent pathways, we used an approach that combines large-scale bioreactor cell culture with tandem affinity purification and mass spectrometry: “bioreactor-TAP-MS/MS.” By applying this approach systematically to all four components of the hypusine modification system (eIF-5A1, eIF-5A2, DHS, and DOHH), we identified 248 interacting proteins as components of the cellular hypusine network, with diverse functions including regulation of translation, mRNA processing, DNA replication, and cell cycle regulation. Network analysis of this data set enabled us to provide a comprehensive overview of the protein-protein interaction landscape of the hypusine modification system. In addition, we validated the interaction of eIF-5A with some of the newly identified associated proteins in more detail. Our analysis has revealed numerous novel interactions, and thus provides a valuable resource for understanding how this crucial homeostatic signaling pathway affects different cellular functions. |
format | Online Article Text |
id | pubmed-3494187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-34941872012-11-09 Protein-protein-interaction Network Organization of the Hypusine Modification System Sievert, Henning Venz, Simone Platas-Barradas, Oscar Dhople, Vishnu M. Schaletzky, Martin Nagel, Claus-Henning Braig, Melanie Preukschas, Michael Pällmann, Nora Bokemeyer, Carsten Brümmendorf, Tim H. Pörtner, Ralf Walther, Reinhard Duncan, Kent E. Hauber, Joachim Balabanov, Stefan Mol Cell Proteomics Research Hypusine modification of eukaryotic initiation factor 5A (eIF-5A) represents a unique and highly specific post-translational modification with regulatory functions in cancer, diabetes, and infectious diseases. However, the specific cellular pathways that are influenced by the hypusine modification remain largely unknown. To globally characterize eIF-5A and hypusine-dependent pathways, we used an approach that combines large-scale bioreactor cell culture with tandem affinity purification and mass spectrometry: “bioreactor-TAP-MS/MS.” By applying this approach systematically to all four components of the hypusine modification system (eIF-5A1, eIF-5A2, DHS, and DOHH), we identified 248 interacting proteins as components of the cellular hypusine network, with diverse functions including regulation of translation, mRNA processing, DNA replication, and cell cycle regulation. Network analysis of this data set enabled us to provide a comprehensive overview of the protein-protein interaction landscape of the hypusine modification system. In addition, we validated the interaction of eIF-5A with some of the newly identified associated proteins in more detail. Our analysis has revealed numerous novel interactions, and thus provides a valuable resource for understanding how this crucial homeostatic signaling pathway affects different cellular functions. The American Society for Biochemistry and Molecular Biology 2012-11 2012-08-10 /pmc/articles/PMC3494187/ /pubmed/22888148 http://dx.doi.org/10.1074/mcp.M112.019059 Text en © 2012 by The American Society for Biochemistry and Molecular Biology, Inc. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles |
spellingShingle | Research Sievert, Henning Venz, Simone Platas-Barradas, Oscar Dhople, Vishnu M. Schaletzky, Martin Nagel, Claus-Henning Braig, Melanie Preukschas, Michael Pällmann, Nora Bokemeyer, Carsten Brümmendorf, Tim H. Pörtner, Ralf Walther, Reinhard Duncan, Kent E. Hauber, Joachim Balabanov, Stefan Protein-protein-interaction Network Organization of the Hypusine Modification System |
title | Protein-protein-interaction Network Organization of the Hypusine Modification System |
title_full | Protein-protein-interaction Network Organization of the Hypusine Modification System |
title_fullStr | Protein-protein-interaction Network Organization of the Hypusine Modification System |
title_full_unstemmed | Protein-protein-interaction Network Organization of the Hypusine Modification System |
title_short | Protein-protein-interaction Network Organization of the Hypusine Modification System |
title_sort | protein-protein-interaction network organization of the hypusine modification system |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494187/ https://www.ncbi.nlm.nih.gov/pubmed/22888148 http://dx.doi.org/10.1074/mcp.M112.019059 |
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