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Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice
Eighty-eight rice (Oryza sativa) cDNAs encoding rice leaf expressed protein kinases (PKs) were fused to a Tandem Affinity Purification tag (TAP-tag) and expressed in transgenic rice plants. The TAP-tagged PKs and interacting proteins were purified from the T1 progeny of the transgenic rice plants an...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723914/ https://www.ncbi.nlm.nih.gov/pubmed/19690613 http://dx.doi.org/10.1371/journal.pone.0006685 |
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author | Rohila, Jai S. Chen, Mei Chen, Shuo Chen, Johann Cerny, Ronald L. Dardick, Christopher Canlas, Patrick Fujii, Hiroaki Gribskov, Michael Kanrar, Siddhartha Knoflicek, Lucas Stevenson, Becky Xie, Mingtang Xu, Xia Zheng, Xianwu Zhu, Jian-Kang Ronald, Pamela Fromm, Michael E. |
author_facet | Rohila, Jai S. Chen, Mei Chen, Shuo Chen, Johann Cerny, Ronald L. Dardick, Christopher Canlas, Patrick Fujii, Hiroaki Gribskov, Michael Kanrar, Siddhartha Knoflicek, Lucas Stevenson, Becky Xie, Mingtang Xu, Xia Zheng, Xianwu Zhu, Jian-Kang Ronald, Pamela Fromm, Michael E. |
author_sort | Rohila, Jai S. |
collection | PubMed |
description | Eighty-eight rice (Oryza sativa) cDNAs encoding rice leaf expressed protein kinases (PKs) were fused to a Tandem Affinity Purification tag (TAP-tag) and expressed in transgenic rice plants. The TAP-tagged PKs and interacting proteins were purified from the T1 progeny of the transgenic rice plants and identified by tandem mass spectrometry. Forty-five TAP-tagged PKs were recovered in this study and thirteen of these were found to interact with other rice proteins with a high probability score. In vivo phosphorylated sites were found for three of the PKs. A comparison of the TAP-tagged data from a combined analysis of 129 TAP-tagged rice protein kinases with a concurrent screen using yeast two hybrid methods identified an evolutionarily new rice protein that interacts with the well conserved cell division cycle 2 (CDC2) protein complex. |
format | Text |
id | pubmed-2723914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27239142009-08-19 Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice Rohila, Jai S. Chen, Mei Chen, Shuo Chen, Johann Cerny, Ronald L. Dardick, Christopher Canlas, Patrick Fujii, Hiroaki Gribskov, Michael Kanrar, Siddhartha Knoflicek, Lucas Stevenson, Becky Xie, Mingtang Xu, Xia Zheng, Xianwu Zhu, Jian-Kang Ronald, Pamela Fromm, Michael E. PLoS One Research Article Eighty-eight rice (Oryza sativa) cDNAs encoding rice leaf expressed protein kinases (PKs) were fused to a Tandem Affinity Purification tag (TAP-tag) and expressed in transgenic rice plants. The TAP-tagged PKs and interacting proteins were purified from the T1 progeny of the transgenic rice plants and identified by tandem mass spectrometry. Forty-five TAP-tagged PKs were recovered in this study and thirteen of these were found to interact with other rice proteins with a high probability score. In vivo phosphorylated sites were found for three of the PKs. A comparison of the TAP-tagged data from a combined analysis of 129 TAP-tagged rice protein kinases with a concurrent screen using yeast two hybrid methods identified an evolutionarily new rice protein that interacts with the well conserved cell division cycle 2 (CDC2) protein complex. Public Library of Science 2009-08-19 /pmc/articles/PMC2723914/ /pubmed/19690613 http://dx.doi.org/10.1371/journal.pone.0006685 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Rohila, Jai S. Chen, Mei Chen, Shuo Chen, Johann Cerny, Ronald L. Dardick, Christopher Canlas, Patrick Fujii, Hiroaki Gribskov, Michael Kanrar, Siddhartha Knoflicek, Lucas Stevenson, Becky Xie, Mingtang Xu, Xia Zheng, Xianwu Zhu, Jian-Kang Ronald, Pamela Fromm, Michael E. Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice |
title | Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice |
title_full | Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice |
title_fullStr | Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice |
title_full_unstemmed | Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice |
title_short | Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice |
title_sort | protein-protein interactions of tandem affinity purified protein kinases from rice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723914/ https://www.ncbi.nlm.nih.gov/pubmed/19690613 http://dx.doi.org/10.1371/journal.pone.0006685 |
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