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on high-resolution cryo-electron microscopy to determine the structures of lipidic alpha-synuclein (αSyn) amyloid fibrils. The aggregation of αSyn as well as its interaction with lipid membranes play a key
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between chemistry and biochemistry. It is structured around two parallel PhD projects: one in chemistry (the position offered) and one in biochemistry, supervised by partner research team. This organization
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for power electronics, RF amplifiers, and motor drives. By incorporating vertical structures, these devices achieve high current handling capabilities while maintaining efficient thermal management
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VCP/p97 conformational dynamics. By combining computational protein design with biochemical experiments and high‑resolution cryo-EM, the project aims to reveal how these binders reshape the structure
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, by integrating image analysis and docking across multiple structural states. The new tools will be validated through their application to VCP/p97 data, a key protein that plays a central role in
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PhD position: Nanoengineering refractory compositionally complex alloys for extreme conditions (M/F)
microscopy (SEM) experiments will be used to identify deformation mechanisms and establish structure–property relationships. At the University of Arizona (U of A), state-of-the-art nanoscale characterization
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reactive CO2 capture systems with structural flexibility, tunable surface properties, thermal stability, and high metal dispersion for the conversion of CO2 into methanol and C2+ alcohols. The research will
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Inria, the French national research institute for the digital sciences | Villers les Nancy, Lorraine | France | 15 days ago
expertise in artificial intelligence, computational chemistry, structural biology, and experimental validation. Biomolecular function depends on both structure and dynamics. In particular, allostery is a
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laser pulses to create (periodic) assemblies of nanosized chiral spin textures on demand. These tunable structures are predicted to host topological spin waves, and will provide a unique playground to
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antibiotic resistance. Until now, cytochrome bd structures from from four different species (E. Coli, Mycobacterium smegmatis, Mycobacterium tuberculosis et Corynebacterium glutamicum) are available. The first