Last modification : Tuesday, December 6, 2022
Jointly appointed Phd position at VIB Switch Laboratory and VIB Laboratory for Neurophysiology in Neurodegenerative Disorders. About the Switch laboratory The SWITCH Laboratory, part of the KUL Department of Cellular and Molecular Medicine and the VIB-KU Leuven Center for Brain & Disease Research, is one of the leading laboratories in human disease-related protein aggregation. It is an interdisciplinary workplace, bringing together about twenty-five researchers from different backgrounds, such as bioinformatics, biophysics and cell biology. SWITCH has a unique platform of technologies for studying protein aggregation, including biophysical, ultrastructural and cell biological instrumentations. For a primer on who we are, what we do and our latest publications, see https:// www. switchlab.org/. About the Da Cruz Laboratory of Neurophysiology in Neurodegenerative Disorders The Da Cruz Laboratory, part of the KUL Department of Neurosciences and the VIB-KU Leuven Center for Brain & Disease Research investigates disease mechanisms for therapy development to ultimately treat ALS and FTD. We focus on the role of local axonal translation and liquid-liquid phase separation/aggregation as well as spreading of disease-associated RNA binding proteins TDP-43 and FUS in axonal/synaptic maintenance and loss. To unravel novel disease targets, we combine sophisticated mouse models, human stem cell and genome editing approaches to model ALS and FTD, together with state-of-the-art spatial omics technologies and high-resolution microscopy. We are a stimulating international team bringing together postdocs, PhD and Master students and lab technicians. See https: // dacruzlab.sites.vib.be/en to learn more about us.Project
TDP-43 aggregation is the major hallmark of nearly all amyotrophic lateral sclerosis (ALS) forms and half of frontotemporal dementia (FTD) cases.
Two leading labs are teaming up and combining their expertise to decipher the molecular underpinnings of TDP-43 aggregation. The Da Cruz lab has innovative cellular systems that recapitulate human TDP-43 pathology as seen in patients and the SWITCH lab has unraveled the importance of heterotypic interactions in amyloid proteins. These tools will be powerfully combined in this project to investigate specific (heterotypic) interactions between the aggregation- prone regions of TDP-43 and the background proteome and to determine which cells are most sensitive to TDP-43 aggregation.
This hypothesis will be tested by performing a genome-wide CRISPR and compound screen in a reporter cell line and followed by computational modelling. The most promising hits will then be validated using a combination of biophysical and biochemical techniques as well as cellular functional assays relevant for disease. You will learn to produce disease-aggregation prone-protein including TDP-43 aggregates recombinantly, as well as isolate them directly from the brains of animal models and human donors. The seeding capacity of TDP-43 aggregates will be studied comprehensively in vitro , in cells and in animal models.Profile
VIB an excellence-based research institute KU Leuven, one of Europe's leading research universities
For more information please contact Prof. dr. Joost Schymkowitz, tel.: +32 16 37 25 73, mail: firstname.lastname@example.org or Mrs. Hannah Wilkinson, tel.: +32 16 37 25 70, mail: email@example.com.
Please complete the online application procedure and include a detailed CV including list of publications, a motivation letter, and the contact information of three referees.
https:// www. switchlab.org/
https: // dacruzlab.sites.vib.be/en
https: // cbd.vib.be
https: // gbiomed.kuleuven.be/english/research/50000618
https: // gbiomed.kuleuven.be/english/research/50000666
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