Project description
We are seeking a highly motivated PhD student to join our research group investigating the cellular mechanisms that protect against (toxic) protein aggregation. A hallmark of neurodegenerative diseases, such as Alzheimer’s disease, Parkinson’s disease, ALS and polyglutamine diseases like Huntington’s disease are protein aggregates in the central nervous system. Our group is studying how protein aggregate formation can be inhibited and how these toxic aggregates are cleared, important aspects to find potential disease ameliorating targets for future therapeutic approaches.
We recently discovered that protein aggregates are degraded via selective autophagy (aggrephagy), but only if they were fragmented beforehand (https://doi.org/10.1038/s41556-025-01747-1). In this study, we identified the players of the fragmentase that are involved, but the precise mechanism of action and the dynamics of this aggregate fragmentation are unsolved. This project builds on that recent discovery and aims at deciphering the molecular mechanisms underlying the functional properties of this fragmentase. We will investigate how the fragmentation of aggregates and the subsequent autophagic clearance cooperate and whether simultaneous stimulation of these processes increases aggregate clearance. This project will employ a combination of advanced cell biology, molecular biology, live-cell imaging, and proteomics approaches.
Your responsibilities will include:
- coordinating and carrying out a scientific research project.
- actively participating in multidisciplinary meetings and project teams.
- developing and optimizing experimental procedures and conduct literature review.
- supervising science rotations of Bachelor and Master students.