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PhD Position: Molecular mechanisms of neurodegenerative diseases; m​/f​/d

in 55116, Mainz, Rheinland-Pfalz, Deutschland
Unternehmen: EURAXESS Czech Republic
Vollzeit, Saisonal/Temporär position
Verfasst am 2026-02-20
Berufliche Spezialisierung:
  • Forschung/Entwicklung
    Forschungswissenschaftler, Klinische Forschung, Medizinwissenschaft
Gehalts-/Lohnspanne oder Branchenbenchmark: 60000 - 80000 EUR pro Jahr EUR 60000.00 80000.00 YEAR
Stellenbeschreibung
Stellenbezeichnung: PhD Position: Molecular mechanisms of neurodegenerative diseases (m/f/d)

Organisation/Company International PhD Programme (IPP) Mainz Department Institute of Molecular Biology Research Field Biological sciences » Biology Researcher Profile First Stage Researcher (R1) Positions PhD Positions Final date to receive applications 1 Apr 2026 - 12:00 (Europe/Berlin) Country Germany Type of Contract Temporary Job Status Full-time Offer Starting Date 1 Jul 2026 Is the job funded through the EU Research Framework Programme?

Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No

Offer Description

Thinking of doing your PhD in the Life Sciences? The International PhD Programme (IPP) Mainz is offering talented scientists the chance to work on cutting edge research projects within the open call on “Molecular Mechanisms in Genome Stability & Gene Regulation” . As an IPP PhD student, you will join a community of exceptional scientists working on diverse topics ranging from how organisms age or how our DNA is repaired, to how epigenetics regulates cellular identity or neural memory.

Activities and responsibilities

The research group of Dorothee Dormann offers the following PhD project:

In the Dormann lab, we study how RNA-binding proteins (RBPs), such as TDP-43, FUS or TAF
15, become dysfunctional in diseases such as amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD) and Alzheimer’s disease (AD). These RBPs function in various RNA metabolic pathways, including the regulation of transcription, pre-mRNA splicing, mRNA stability and translation as well as in DNA damage repair. A subset of patients with ALS, FTD and AD present pathological cytoplasmic redistribution and aggregation of TDP-43, FUS or TAF
15, however it is still not well understood how these proteins become mislocalized and aggregated in disease and how RBP aggregation causes a decline in cellular function and eventually neurodegeneration.

PhD project:
Role of cellular mechanical stress in RNA-binding protein aggregation diseases

We and others previously showed that different types of cellular stress, e.g. oxidative stress or heat shock, elicit recruitment of RBPs into stress granules (SGs) and that SGs and aberrant phase transitions can lead to pathological TDP-43 or FUS aggregation. In this project, we now want to focus on mechanical stress and investigate how it impacts RBP mislocalization and aggregation. We will apply mechanical stress, e.g. through mechanical agitation or by applying shear forces in microfluidic devices, and will investigate how this impacts phase separation and aggregation of TDP-43, FUS or TAF
15 in vitro. We will also apply mechanical stress to cells and will investigate how (in comparison to other cellular stressors) it impacts nucleocytoplasmic transport and the formation of SGs, and hence cytoplasmic mislocalization and aggregation of RBPs, such as TDP-43, FUS or TAF
15. We also seek to investigate how the presence of aggregates in cells impacts the mechanical properties of cells, e.g. changes to the viscoelasticity of the cytoplasm and/or nuclear shape.

To address these questions, we will use recombinant proteins to study phase separation/aggregation in vitro, e.g. with microscopic or biophysical assays, as well as cell lines and neuronal cell culture models to study the intracellular RBP behaviour using diverse imaging techniques (e.g. confocal microscopy, live cell imaging) combined with biochemical and cell biological methods or proteomics.

The PhD project is part of the EU-funded doctoral training network “NEUROMECH”, which seeks to characterize the role of mechanobiology in the pathogenesis of neurodegenerative diseases. Investigators in the consortium have expertise in mechanobiology, neurodegeneration, DNA damage, neuropathology, medical imaging and big data analysis. Students will profit from lab exchanges and diverse training activities within the NEUROMECH network.

If you are interested in this project, please select
Dormann
as your group preference in the IPP application platform.

Qualification profile:

Are you an ambitious scientist looking to push the boundaries of research while interacting with colleagues from multiple…

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