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Project PartnersPD Dr. Michael SchrodaUniversity of Potsdam, Institute of Biochemistry and Biology/Genetics c/o Max Planck Institute of Molecular Plant Physiology Core Competency: Protein identification and quantification based on mass spectrometry, stable isotope labelling and 15NH4Cl labelling. Metabolite profiling using GC-TOF-MS. Chromatin immunoprecipitation. Analysis of protein-protein interactions. Transgene expression and RNAi approaches in Chlamydomonas. Gene identification. Long-standing experience with Chlamydomonas (member of the DFG-funded consortium FOR504, co-author of the current Chlamydomonas Sourcebook). Contribution to Work Programme: Large scale analysis of changes in metabolite and protein levels following well-defined changes in growth conditions (WP2 and 3). Genetic manipulations of Chlamydomonas for refinement and testing of models developed in WP1.4. Target sites for key transcription factors on a genome-wide scale will be identified by ChIP-seq. GoFORSYS Publications of the Group: (incl. thosey former Group Leader Wolfram Weckwerth) Hummel, J., M. Niemann, et al. (2007). "ProMEX: a mass spectral reference database for proteins and protein phosphorylation sites." Bmc Bioinformatics 8: -. Merchant, S. S., S. E. Prochnik, et al. (2007). "The Chlamydomonas genome reveals the evolution of key animal and plant functions." Science 318(5848): 245-251. Muller-Linow, M., Weckwerth, W., and Hutt, M. T. (2007) Consistency analysis of metabolic correlation networks. Bmc Systems Biology 1, -. Reumann, S., L. Babujee, et al. (2007). "Proteome analysis of Arabidopsis leaf peroxisomes reveals novel targeting peptides, metabolic pathways, and defense mechanisms." Plant Cell 19(10): 3170-3193. Heazlewood, J. L., P. Durek, et al. (2008). "PhosPhAt: a database of phosphorylation sites in Arabidopsis thaliana and a plant-specific phosphorylation site predictor." Nucleic Acids Research 36: D1015-D1021 Heide, H., A. Nordhues, et al. (2008). "Application of quantitative mass spectrometry combined with immunoprecipitation, knock-down and cross- linking (QUICK-X) to Chlamydomonas reveals the interaction of VIPP1 with chloroplast SP90C." Proteomics. Hoehenwarter, W., J. T. van Dongen, et al. (2008). "A rapid approach for phenotype-screening and database independent detection of cSNP/protein polymorphism using mass accuracy precursor alignment." Proteomics 8(20): 4214-4225. Lehmann, U., S. Wienkoop, et al. (2008). "If the antibody fails - a mass Western approach." Plant Journal 55(6): 1039-1046. Weckwerth, W. (2008). Metabolomics und Datenintegration in der Systembiologie, BMBF. Weckwerth, W. (2008). "Integration of metabolomics and proteomics in molecular plant physiology - coping with the complexity by data-dimensionality reduction." Physiologia Plantarum 132(2): 176-189. Weckwerth, W. (2008). Metabolomics und Datenintegration in der Systembiologie, BMBF. Wienkoop, S., K. Morgenthal, et al. (2008). "Integration of metabolomic and proteomic phenotypes." Molecular & Cellular Proteomics 7(9): 1725-1736. Kempa, S., J. Hummel, et al. (2009). "An automated GCxGC-TOF-MS protocol for batch-wise extraction and alignment of mass isotopomer matrixes from differential C-13-labelling experiments: a case study for photoautotrophic-mixotrophic grown Chlamydomonas reinhardtii cells." Journal of Basic Microbiology 49(1): 82-91. Â |
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