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Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets
14-3-3 proteins are a family of ubiquitous dimeric proteins that modulate many cellular functions in all eukaryotes by interacting with target proteins. 14-3-3s exist as a number of isoforms that in Arabidopsis identifies two major groups named ε and non-ε. Although isoform specificity has been demo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946203/ https://www.ncbi.nlm.nih.gov/pubmed/24603559 http://dx.doi.org/10.1371/journal.pone.0090764 |
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author | Pallucca, Roberta Visconti, Sabina Camoni, Lorenzo Cesareni, Giovanni Melino, Sonia Panni, Simona Torreri, Paola Aducci, Patrizia |
author_facet | Pallucca, Roberta Visconti, Sabina Camoni, Lorenzo Cesareni, Giovanni Melino, Sonia Panni, Simona Torreri, Paola Aducci, Patrizia |
author_sort | Pallucca, Roberta |
collection | PubMed |
description | 14-3-3 proteins are a family of ubiquitous dimeric proteins that modulate many cellular functions in all eukaryotes by interacting with target proteins. 14-3-3s exist as a number of isoforms that in Arabidopsis identifies two major groups named ε and non-ε. Although isoform specificity has been demonstrated in many systems, the molecular basis for the selection of specific sequence contexts has not been fully clarified. In this study we have investigated isoform specificity by measuring the ability of different Arabidopsis 14-3-3 isoforms to activate the H(+)-ATPase. We observed that GF14 isoforms of the non-ε group were more effective than ε group isoforms in the interaction with the H(+)-ATPase and in the stimulation of its activity. Kinetic and thermodynamic parameters of the binding of GF14ε and GF14ω isoforms, representative of ε and non-ε groups respectively, with the H(+)-ATPase, have been determined by Surface Plasmon Resonance analysis demonstrating that the higher affinity of GF14ω is mainly due to slower dissociation. The role of the C-terminal region and of a Gly residue located in the loop 8 and conserved in all non-ε isoforms has also been studied by deletion and site-specific mutagenesis. The C-terminal domains, despite their high divergence, play an auto-inhibitory role in both isoforms and they, in addition to a specific residue located in the loop 8, contribute to isoform specificity. To investigate the generality of these findings, we have used the SPOT-synthesis technology to array a number of phosphopeptides matching known or predicted 14-3-3 binding sites present in a number of clients. The results of this approach confirmed isoform specificity in the recognition of several target peptides, suggesting that the isoform specificity may have an impact on the modulation of a variety of additional protein activities, as suggested by probing of a phosphopeptide array with members of the two 14-3-3 groups. |
format | Online Article Text |
id | pubmed-3946203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39462032014-03-12 Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets Pallucca, Roberta Visconti, Sabina Camoni, Lorenzo Cesareni, Giovanni Melino, Sonia Panni, Simona Torreri, Paola Aducci, Patrizia PLoS One Research Article 14-3-3 proteins are a family of ubiquitous dimeric proteins that modulate many cellular functions in all eukaryotes by interacting with target proteins. 14-3-3s exist as a number of isoforms that in Arabidopsis identifies two major groups named ε and non-ε. Although isoform specificity has been demonstrated in many systems, the molecular basis for the selection of specific sequence contexts has not been fully clarified. In this study we have investigated isoform specificity by measuring the ability of different Arabidopsis 14-3-3 isoforms to activate the H(+)-ATPase. We observed that GF14 isoforms of the non-ε group were more effective than ε group isoforms in the interaction with the H(+)-ATPase and in the stimulation of its activity. Kinetic and thermodynamic parameters of the binding of GF14ε and GF14ω isoforms, representative of ε and non-ε groups respectively, with the H(+)-ATPase, have been determined by Surface Plasmon Resonance analysis demonstrating that the higher affinity of GF14ω is mainly due to slower dissociation. The role of the C-terminal region and of a Gly residue located in the loop 8 and conserved in all non-ε isoforms has also been studied by deletion and site-specific mutagenesis. The C-terminal domains, despite their high divergence, play an auto-inhibitory role in both isoforms and they, in addition to a specific residue located in the loop 8, contribute to isoform specificity. To investigate the generality of these findings, we have used the SPOT-synthesis technology to array a number of phosphopeptides matching known or predicted 14-3-3 binding sites present in a number of clients. The results of this approach confirmed isoform specificity in the recognition of several target peptides, suggesting that the isoform specificity may have an impact on the modulation of a variety of additional protein activities, as suggested by probing of a phosphopeptide array with members of the two 14-3-3 groups. Public Library of Science 2014-03-06 /pmc/articles/PMC3946203/ /pubmed/24603559 http://dx.doi.org/10.1371/journal.pone.0090764 Text en © 2014 Pallucca et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pallucca, Roberta Visconti, Sabina Camoni, Lorenzo Cesareni, Giovanni Melino, Sonia Panni, Simona Torreri, Paola Aducci, Patrizia Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets |
title | Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets |
title_full | Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets |
title_fullStr | Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets |
title_full_unstemmed | Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets |
title_short | Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H(+)-ATPase and Other Targets |
title_sort | specificity of ε and non-ε isoforms of arabidopsis 14-3-3 proteins towards the h(+)-atpase and other targets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946203/ https://www.ncbi.nlm.nih.gov/pubmed/24603559 http://dx.doi.org/10.1371/journal.pone.0090764 |
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