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AIAS-COFUND (Marie Curie) Fellowships

Aarhus Institute of Advanced Studies (AIAS) AIAS-COFUND Fellowships are available for talented researchers. The scheme is co-funded by Aarhus University's Research Foundation and the European Union’s 7th Framework Programme under grant agreement no 609033 and provides research opportunities for the most talented researchers from around the world.

1 Oct 2019 - 30 Sep 2022  

Project: Molecular innovation in genetic conflicts

Regulation of gene expression forms the foundation for basic cellular processes, development and disease in multicellular organisms. During my postdoctoral work in Vienna, I discovered that animal genomes, through rapid ‘arms race’ evolution, evolve new molecular mechanisms that allow the cell to bend and bypass the textbook rules of gene expression. Such ‘hacked’ gene expression produces RNA molecules that are essential for animals to combat genetic parasites such as transposons (‘jumping genes’). With my AIAS fellow project, I will build on these new concepts to identify the molecular mechanisms underlying ‘hacked’ genome expression, 2) investigate the connection between transposon silencing and general regulation of the genome. To address these questions, I will combine genetic manipulation of both in vivo models (Drosophila) and cell culture systems with molecular analysis using diverse genomics approaches. With my research as AIAS fellow I aim to pioneer the emerging field of heterochromatin-based expression mechanisms and uncover new modes of genome regulation during animal development and disease. 


Project: How do we sense touch, sound, balance and force?

Project description

Perception of force is a key component in our sense of touch, hearing, balance and pain as well as in regulation of blood and osmotic pressures. Fundamental to these concepts is that at some point force (newtons) is translated into electrical conductance (siemens) through the action of membrane embedded mechanosensitive channels that open or closes in response to changing forces in the lipid bilayer. Conceptually this is perfectly conceivable, but it is astonishingly little we know about the mechanism of how bilayer responses are converted into changes in channel activity. So unlike the well-described nature of taste and odorant receptors and the photoreceptors in the eye, we have not yet a clear idea of how our mechanosensitive receptors work.

When studying the relationship between lipid membrane and embedded proteins the major challenge is that, in contrast to stimulation with e.g. ligands or voltage, we don’t really know the exact nature of our stimulation; we can poke or pull a cell, but we cannot quantify what the channel actually feels at a molecular level.

To increase our understanding of functional interactions between lipids and protein, we will use a minimalist approach by developing novel assays that utilize a set of molecular tools to manipulate specific forces in the membrane, while at the same time taking advantage of the detailed information available from singe channel recordings. 


Project: Can a cooked noodle store information? The mechanisms of disordered proteins in synaptic plasticity

Learning and memory depends on the ability to modulate the connections between neurons in the brain in a process called synaptic plasticity. An important mechanism in synaptic plasticity involves the proteins sensing chemical signals at synapses, neurotransmitter receptors. The NMDA receptor is a neurotransmitter receptor with a key role in learning, which depends on its large intracellular domains. The intracellular domains are intrinsically disordered, are the target of many kinases and bind to many other proteins. Despite its importance, we know little about how the intracellular domains regulate the receptor mechanistically, and little about how intrinsically disordered proteins can exert long-range regulatory effects in general. This is largely due to the almost complete lack of structural information on the intra-cellular domains.

In this project, I will study the intracellular domains of the NMDA receptor using a combination of NMR spectroscopy and single molecule FRET. Structural experiments will be complemented by functional measurements using electrophysiology in Xenopus oocytes. The goal is to identify the mechanism by which the intra-cellular domains affect synaptic plasticity on short time-scales, and how this effect is modulated by phosphorylations and ligand interactions. This will provide another piece of the enigma of how the many wonderful functions of the brain emerge from chemical and physical processes.


Projekt: Mekanismer bag kolesterol og sukkeroptag

Bjørn Panyella Pedersens forskning er fokuseret på to aspekter af menneskers fødevareoptag. For det første vil Bjørn og hans nye forskningsgruppe ved Institut for Molekylærbiologi og Genetik undersøge, hvordan kroppen optager kolesterol fra tyndtarmen. Kolesterol i store mængder kan lede til hjertekarsygdomme, men kolesterol er absolut essentielt for en velfungerende krop i moderate mængder. Kolesterol optages i tyndtarmen til kroppens kredsløb ved hjælp af et protein kaldet NPC1L1.