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advancements. In this project, we aim to develop cutting-edge XL–MS methods to elucidate the structural organization of protein complexes critical to microbial virulence. We focus on studying the type VI
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structure and function of cellular RNA polymerase transcription complexes using cryo-electron microscopy, biophysics, and biochemical methods. Applicants must hold a PhD in biochemistry, biophysics
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the preparation of reports, structural justifications, and research documentation. Capacity to work with complex geometries and to collaborate with multidisciplinary teams (materials, digital fabrication, design
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Dendooven Lab — VIB–VUB Center for Structural Biology (CSB), Brussels, Belgium Start date: March–May 2026 | Duration: 4 years | Funding: ERC Starting Grant Description We are seeking a postdoctoral
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and structural transitions of transcription complexes and transcription-translation complexes and to identify and characterize small-molecule inhibitors of transcription. Prepares and assays proteins
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leading therapeutic target. The project emphasizes cryo-EM structural studies to characterize LRRK2 signaling in disease states and identify novel therapeutic strategies for PD. Ideal Candidate We seek a
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-resolution structures of bacterial immune complexes using single-particle cryo-electron microscopy. Prepare, purify, and characterize protein complexes, including large multi-subunit assemblies and membrane
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reconstitution, and single-particle cryo-EM analysis of membrane protein complexes, as well as structural–functional assays in human cells. The exact project will be developed together with the selected researcher
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Position Details Position Information Recruitment/Posting Title Postdoctoral Associate in Structural Biology and Biophysics Department Quantitative Biomedicine Inst Salary Details 63968 Offer
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The International Institute of Molecular Mechanisms and Machines Polish Academy of Sciences | Poland | about 5 hours ago
the structural mechanisms of protein transport into and across the inner mitochondrial membrane, governed by the complex protein translocase called TIM23. The progress achieved to date in this area has defined