mt proteomcis, symbiotic proteomics of Medicago truncatula

MT proteomics
bulle MT Proteomics Home page
Summary of the project
Perspectives
References
Links
bas

FLASH / NEWS
Biofutur, revue
Voir notre article dans cette revue
bas



2. Sub-cellular membrane proteomics

Our second task was aimed at developing different sub-cellular proteomic analyses in order to have access to membrane proteins of the fully established AM symbiosis.

2b. Comparative extrinsic membrane proteomics of the AM symbiosis

Membrane proteins were extracted from M. truncatula roots either inoculated or not with the AM fungus G. intraradices. Comparative two-dimensional electrophoresis revealed that 36 spots were differentially displayed in response to the fungal colonization including 15 proteins induced, 3 up-regulated and 18 down-regulated. Among them, seven proteins were found to be commonly down-regulated in AM-colonized and phosphate-fertilized roots. Twenty-five spots out of the 36 of interest could be identified by matrix assisted laser desorption/ionisation-time of flight and/or tandem mass spectrometry analyses.
Excepting an acid phosphatase and a lectin, none of them was previously reported as being regulated during AM symbiosis. In addition, this proteomic approach allowed us for the first time to identify AM fungal proteins in planta.

Click on the reference map


retour haut de pageTop
Réalisation - 2005 Number of visitors 40365 
Last modified Thu 09 Sep 2010 3:35 AM Mt proteomics.com mt proteomics - truncatulaWebmaster- JM-Conseil
universite de bourgogne  INRA CNRS