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(PER1,2,3) and Cryptochrome (CRY1,2) clock proteins, which feedback-repress CLOCK/BMAL1. Within a 24h day, CLOCK/BMAL1 cycles between an active state recruiting co-activators like MLL1, an early repressed
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. The doctoral project focuses on the question of how plastidial GNATs interact with RNA-binding proteins (RBPs) and co-localize in phase-separated plastidial condensates to enable targeted protein acetylation
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interactions. We develop and apply chemical biology methods – including chemical probe synthesis, protein biochemistry and chemical proteomics – to understand the impact of bacterial enzymes on multipartite
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a dynamic, growing team in the field of enzyme and protein design Collaborate in the context of a prestigious DFG Priority Programme (SPP2363) Enjoy a vibrant scientific environment at the Weinberg
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-HEART Consortium: Method development to quantify very low-concentrated proteins in human blood plasma, e.g. using targeted LC-/MS/MS methods to detect interleukins Continuous development of existing
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-HEART Consortium: Method development to quantify very low-concentrated proteins in human blood plasma, e.g. using targeted LC-/MS/MS methods to detect interleukins Continuous development of existing
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genetic information into functional proteins, regulating gene expression, and coordinating cellular responses. Like DNA, RNA is vulnerable to chemical damage from endogenous metabolic byproducts and
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RNA-binding proteins (RBPs), such as TDP-43, FUS or TAF15, become dysfunctional in diseases such as amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD) and Alzheimer’s disease (AD
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. BioRxiv 2024; doi: https://doi.org/10.1101/2024.04.15.589474 ). In this PhD project, we will validate these molecules and interrogate their mechanism of action using confocal microscopy, protein chemistry
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for a fully funded PhD position within the DFG Priority Programme SPP2389 https://tu-dresden.de/mn/biologie/allgemeine_mikrobiologie/spp2389 . International collaboration The PhD is embedded in a close