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Field
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encoded FRET biosensors for mitochondrial functionality. - Implement innovative data analysis protocols and approaches for FRET/FLIM or radiometric FRET microscopy in cultured cell lines - Modify and/or
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flux de l'eau du circuit primaire, les tubes en 316LN subissent des vibrations induites par les écoulements turbulents. Ces vibrations engendrent des micro-glissements alternés (fretting), combinés à des
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binding assays, bioluminescent and fluorescent resonance energy transfer (BRET/FRET) and proximity ligation assays, protein purification techniques, enzymatic activity assays, PCR/qPCR, DNA cloning. Cell
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allosteric coupling, to exquisitely control signal routing. We integrate structural biology (NMR, X-ray, cryoEM) and biophysical techniques (FRET, ITC, BLI) with cellular readouts (TopFlash, BRET) and
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allosteric coupling, to exquisitely control signal routing. We integrate structural biology (NMR, X-ray, cryoEM) and biophysical techniques (FRET, ITC, BLI) with cellular readouts (TopFlash, BRET) and
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in fluorescence resonance energy transfer (FRET) assay to study protein-protein interactions. Skills for handling biochemical issues and experimental techniques. Good knowledge of the English language
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to characterise binary and ternary complex formation, including TR-FRET, AlphaLISA, SPR (Surface Plasmon Resonance), ITC (Isothermal Titration Calorimetry), and NanoBRET. Pursuing co-crystal structures of BromoTag
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Working with biophysical assay data (e.g. SPR, TR-FRET, AlphaLISA, ITC, NanoBRET) to guide compound design and prioritisation Use of analytical chemistry techniques relevant to probe characterisation (HPLC
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and develop advanced fluorescence and imaging approaches, including FRET-based assays, fluorescence lifetime imaging (FLIM), live-cell microscopy, site-specific bio-orthogonal protein labelling by
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formulation, bioimaging techniques (e.g. confocal microscopy, FRET, FRAP), and/or in vivo studies. Good publication record, communication skills, and ability to conduct independent research. Experience in