International Graduate School of Neuroscience

Research Interests

Most biomolecules function inside the cell. However, biochemical assays and analytical tools are mainly applied in vitro, in aqueous buffer solutions or crystals. Our research aim is to discover novel biochemical function by studying biomolecular reactions directly in cells under health and disease conditions. To analyze biomolecular reactions in vivo with high spatio-temporal resolution, we developed novel in-cell spectroscopic and microscopic techniques that range from temperature-induced relaxation to single molecule spectroscopy. We apply the methods in environments of increasing complexity ranging from cytomimetic media and bacteria to neuronal cells and multicellular organisms. Our current research interest lies in the field of neurodegenerative diseases with a focus on the following research topics.

Protein folding, misfolding and aggregation

Most methods to measure the rates of protein folding and aggregation of disease-related proteins rely on in vitro methods such as ThT binging assays. Using experiments in cytomimetic media, our lab elaborated a novel thermodynamic model to understand how different compounds like ions, metabolies, crowders, drugs or dehydration could modify the underlying equilibria. Using a biosensor framework, we could interpret in-cell folding experiments under physiological conditions, cell stress or differentiation. These insights led to a novel classification of disease-related mutants. We further implemented a novel assay to measure protein aggregation kinetics with high spatio-temporal resolution directly in cells that can be used to screen novel classes of aggregation inhibitors as potential drugs.

Proteostasis and molecular chaperones

Molecular chaperones constitute a cellular mechanism to prevent aggregation and to retain the proteome folded in space and time. We established a novel method to measure proteostasis capacity under various cellular conditions. This work led us to investigate the different mechanisms of chaperones to modify the folding, misfolding and aggregation rates of different protein substrates.

Biomolecular condensates

It is now clear that biomolecular condensates play a profound role in folding, aggregation and amyloid-associated pathologies. Our current work will advance the understanding of functional and dysfunctional condensates by revealing how stress granules, in conjunction with other factors like molecular chaperones, could reshape folding and aggregation pathways to assist protein homeostasis, or conversely, how the integrity of SGs could be endangered by sequestration of different amyloidogenic species.

Enzymatic catalysis

Metabolic enzymes can be spatially and temporally organized in cells forming regulatory multi-enzyme complexes called metabolons. Little is known about such complexes since they cannot be studied by disruptive protocols in vitro. Based on our previous work in which we learned how enzymatic stability and catalysis changes in cytomimetic and cytoplasmic environments compared to dilute solution, we investigate the stability and metabolic activity of enzymes in metabolons.

RNA structure and function

Compared to proteins, little is known about RNA structure and folding in cells. Our lab was first to measure the stability of well-folded RNA hairpins inside cells. In our current research, we focus on disease-relevant RNA sequences like the CAG triplet-repeat RNA hairpin involved in Huntington’s disease.