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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Biochemistry and Molecular Biology 2012
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.
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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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