We are looking for a talented and highly motivated PhD student to join our team.
The assembly of stress granules is an integral part of the host stress response, a central pathway that controls host protein synthesis [1]. Stress granules form by a cytosolic liquid-liquid phase separation event in which stalled mRNAs are separated from the rest of the cytosol along with translation factors and RNA-binding proteins. Stress granules are often observed during viral infections. Our previous research has shown that chronic infection with hepatitis C virus induces a unique temporal control of this stress response, with alternating states of translational arrest and activation accompanied by the assembly and disassembly of cytosolic stress granules [2,3]. Stress granules are dynamic structures that rapidly assemble under various stress conditions and disassemble within minutes as cells recover from stress. However, the formation of persistent stress granules has been implicated in the pathogenesis of stress-related diseases and inflammatory conditions, including cancer and neurodegenerative diseases.
You will be engaged in an ambitious project at the interface of molecular biology and synthetic cell biology. The project aims at investigating the molecular mechanisms involved in stress granule disassembly, including the role of post-translational modifications, in the context of viral infections, immunity, and neurodegenerative diseases. For this, you will combine analyses in living cells with cell-free droplet-based microfluidics approaches. This project will make a major contribution to our molecular understanding of stress granule phase separation and pave the way for the long-term development of therapeutic interventions.
You will use a combination of state-of-the-art cellular and molecular biology techniques, virology techniques, in vitro transcription and in vitro translation methods, confocal-based microscopy, droplet-based microfluidics.
The project benefits from a close collaboration between the Spatz Lab (MPI for Medical Research, Heidelberg), focusing on microfluidics approaches, and the Ruggieri lab, focusing on the biology of stress granules and on the regulation of the integrated stress response. The project is part of a DFG-funded research consortium (SFB1129) on "Integrative Analysis of Pathogen Replication and Spread", embedded within a lively community of scientists in Heidelberg.
We offer an open, dynamic, and challenging work environment where teamwork, initiative and originality are encouraged and valued.
PhD applicants should send their application via the Heidelberg Biosciences International Graduate School (HBIGS) (https://www.hbigs.uni-heidelberg.de/) - Offer Ruggieri-02
References:
1. Eiermann, N., Haneke, K., Sun, Z., Stoecklin, G. & Ruggieri, A. Dance with the Devil: Stress Granules and Signaling in Antiviral Responses. Viruses 12:984 (2020).
2. Ruggieri A, Dazert E, Metz P, Hofmann S, Bergeest JP, Mazur J, Bankhead P, Hiet MS, Kallis S, Alvisi G, Samuel CE, Lohmann V, Kaderali L, Rohr K, Frese M, Stoecklin G, Bartenschlager R. Dynamic oscillation of translation and stress granule formation mark the cellular response to virus infection. Cell Host Microbe 12:71 (2012).
3. Klein, P., Kallenberger, S. M., Roth, H., Roth, K., Ly-Hartig, T. B. N., Magg, V., Ales, J., Talemi, S. R., Qiang, Y., Wolf, S., Oleksiuk, O., Kurilov, R., Di Ventura, B., Bartenschlager, R., Eils, R., Rohr, K., Hamprecht, F. A., Hofer, T., Fackler, O. T., Stoecklin, G. & Ruggieri, A. Temporal control of the integrated stress response by a stochastic molecular switch. Sci Adv 8:eabk2022 (2022).