Kinome profiling of Arabidopsis using arrays of kinase consensus substrates

<p>Abstract</p> <p>Background</p> <p>Kinome profiling aims at the parallel analysis of kinase activities in a cell. Novel developed arrays containing consensus substrates for kinases are used to assess those kinase activities. The arrays described in this paper were alr...

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Main Authors: Pieterse Corné MJ, van Workum Wilbert, Joore Jos, Ritsema Tita
Format: Article
Language:English
Published: BMC 2007-02-01
Series:Plant Methods
Online Access:http://www.plantmethods.com/content/3/1/3
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spelling doaj-17a1c35ec74046e6a8a2af444c1a946b2020-11-24T21:23:50ZengBMCPlant Methods1746-48112007-02-0131310.1186/1746-4811-3-3Kinome profiling of Arabidopsis using arrays of kinase consensus substratesPieterse Corné MJvan Workum WilbertJoore JosRitsema Tita<p>Abstract</p> <p>Background</p> <p>Kinome profiling aims at the parallel analysis of kinase activities in a cell. Novel developed arrays containing consensus substrates for kinases are used to assess those kinase activities. The arrays described in this paper were already used to determine kinase activities in mammalian systems, but since substrates from many organisms are present we decided to test these arrays for the determination of kinase activities in the model plant species <it>Arabidopsis thaliana</it>.</p> <p>Results</p> <p>Kinome profiling using Arabidopsis cell extracts resulted in the labelling of many consensus peptides by kinases from the plant, indicating the usefulness of this kinome profiling tool for plants. Method development showed that fresh and frozen plant material could be used to make cell lysates containing active kinases. Dilution of the plant extract increased the signal to noise ratio and non-radioactive ATP enhances full development of spot intensities.</p> <p>Upon infection of Arabidopsis with an avirulent strain of the bacterial pathogen <it>Pseudomonas syringae </it>pv. <it>tomato</it>, we could detect differential kinase activities by measuring phosphorylation of consensus peptides.</p> <p>Conclusion</p> <p>We show that kinome profiling on arrays with consensus substrates can be used to monitor kinase activities in plants. In a case study we show that upon infection with avirulent <it>P. syringae </it>differential kinase activities can be found. The PepChip can for example be used to purify (unknown) kinases that play a role in <it>P. syringae </it>infection.</p> <p>This paper shows that kinome profiling using arrays of consensus peptides is a valuable new tool to study signal-transduction in plants. It complements the available methods for genomics and proteomics research.</p> http://www.plantmethods.com/content/3/1/3
collection DOAJ
language English
format Article
sources DOAJ
author Pieterse Corné MJ
van Workum Wilbert
Joore Jos
Ritsema Tita
spellingShingle Pieterse Corné MJ
van Workum Wilbert
Joore Jos
Ritsema Tita
Kinome profiling of Arabidopsis using arrays of kinase consensus substrates
Plant Methods
author_facet Pieterse Corné MJ
van Workum Wilbert
Joore Jos
Ritsema Tita
author_sort Pieterse Corné MJ
title Kinome profiling of Arabidopsis using arrays of kinase consensus substrates
title_short Kinome profiling of Arabidopsis using arrays of kinase consensus substrates
title_full Kinome profiling of Arabidopsis using arrays of kinase consensus substrates
title_fullStr Kinome profiling of Arabidopsis using arrays of kinase consensus substrates
title_full_unstemmed Kinome profiling of Arabidopsis using arrays of kinase consensus substrates
title_sort kinome profiling of arabidopsis using arrays of kinase consensus substrates
publisher BMC
series Plant Methods
issn 1746-4811
publishDate 2007-02-01
description <p>Abstract</p> <p>Background</p> <p>Kinome profiling aims at the parallel analysis of kinase activities in a cell. Novel developed arrays containing consensus substrates for kinases are used to assess those kinase activities. The arrays described in this paper were already used to determine kinase activities in mammalian systems, but since substrates from many organisms are present we decided to test these arrays for the determination of kinase activities in the model plant species <it>Arabidopsis thaliana</it>.</p> <p>Results</p> <p>Kinome profiling using Arabidopsis cell extracts resulted in the labelling of many consensus peptides by kinases from the plant, indicating the usefulness of this kinome profiling tool for plants. Method development showed that fresh and frozen plant material could be used to make cell lysates containing active kinases. Dilution of the plant extract increased the signal to noise ratio and non-radioactive ATP enhances full development of spot intensities.</p> <p>Upon infection of Arabidopsis with an avirulent strain of the bacterial pathogen <it>Pseudomonas syringae </it>pv. <it>tomato</it>, we could detect differential kinase activities by measuring phosphorylation of consensus peptides.</p> <p>Conclusion</p> <p>We show that kinome profiling on arrays with consensus substrates can be used to monitor kinase activities in plants. In a case study we show that upon infection with avirulent <it>P. syringae </it>differential kinase activities can be found. The PepChip can for example be used to purify (unknown) kinases that play a role in <it>P. syringae </it>infection.</p> <p>This paper shows that kinome profiling using arrays of consensus peptides is a valuable new tool to study signal-transduction in plants. It complements the available methods for genomics and proteomics research.</p>
url http://www.plantmethods.com/content/3/1/3
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