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Methods for study of plant phosphoproteins
Válková, Martina ; Lochman,, Jan (referee) ; Fohlerová, Radka (advisor)
Reversibly phosphorylated proteins play a role in many fundamental cellular processes. An example is the cytokinin signal transduction pathway in plants that is mediated by the so-called two-component system involving histidine and aspartate phosphorylation. Due to the very low stability of phosphorylation of these amino acids, is difficult to find a suitable method for phosphorylation studies. The theoretical part of this bachelor thesis describes not only the current experimental approaches for analysis of protein phosphorylation in two-component systems but also is trying to propose new approaches for this analysis. There are described methods based on labeling of proteins using [?-32P] ATP and on the detection of released phosphate employing the colorimetric method or ICP-MS. Another possibility is sensitive identification of phoshorylated and non-phosphorylated forms of protein fused with GFP using CE-LIF technique. The practical part of the thesis deals with optimization of the selected colorimetric methods and also is focused on the preparation of the AHP5 protein fused with GFP for CE-LIF analysis.
Methods for study of plant phosphoproteins
Válková, Martina ; Lochman,, Jan (referee) ; Fohlerová, Radka (advisor)
Reversibly phosphorylated proteins play a role in many fundamental cellular processes. An example is the cytokinin signal transduction pathway in plants that is mediated by the so-called two-component system involving histidine and aspartate phosphorylation. Due to the very low stability of phosphorylation of these amino acids, is difficult to find a suitable method for phosphorylation studies. The theoretical part of this bachelor thesis describes not only the current experimental approaches for analysis of protein phosphorylation in two-component systems but also is trying to propose new approaches for this analysis. There are described methods based on labeling of proteins using [?-32P] ATP and on the detection of released phosphate employing the colorimetric method or ICP-MS. Another possibility is sensitive identification of phoshorylated and non-phosphorylated forms of protein fused with GFP using CE-LIF technique. The practical part of the thesis deals with optimization of the selected colorimetric methods and also is focused on the preparation of the AHP5 protein fused with GFP for CE-LIF analysis.

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