Can we remove molecular factors that keep chronic inflammation switched on?
Coordinators: E. Wolf (CAU), P. Rosenstiel (CAU)
Persistent epigenetic changes may keep cells locked in an inflammatory state. Some of the proteins involved in maintaining these changes have been difficult to target with conventional drugs and were previously considered “undruggable”.
TI-5 explores a new technology called PROTACs (proteolysis targeting chimeras). Instead of simply inhibiting a target protein, these molecules use the cell’s own protein-degradation machinery to selectively remove it.
Focusing on inflammatory bowel disease, we will use this approach to identify and target epigenetic factors that may drive chronic inflammation, and investigate whether removing these factors can reprogramme inflammatory cells towards a healthier state.
This could open up new ways of targeting the molecular mechanisms that make inflammation chronic.
Members
Prof. Dr. med. Konrad Aden
Full member
UKSH Campus Kiel
Department of Internal Medicine I
Prof. Dr. rer. nat. Petra Bacher
Full member
UKSH Campus Kiel
Department of Medical Immunology
Prof. Dr. John Baines
Full member
Max Planck Institute for Evolutionary Biology
Institute of Experimental Medicine
Evolutionary Genomics
Prof. Dr. rer. nat. Andreas Hutloff
Full member
UKSH Campus Kiel
Department of Medical Immunology
Prof. Dr. rer. nat. Sabrina Jabs
Full member
Kiel University
Institute of Clinical Molecular Biology
Prof. Dr. rer. nat. Henriette Kirchner
Full member
UKSH Campus Lübeck and Kiel
Department of Human Genetics
AG Epigenetics and Metabolism
Prof. Dr. med. Franz-Josef Müller
Full member
UKSH Campus Kiel
Department of Psychiatry and Psychotherapy
Center for Integrative Psychiatry gGmbH
Prof. Dr. med. Philip Rosenstiel
Full member
Kiel University
Institute of Clinical Molecular Biology
Systems Immunology
Prof. Dr. Elmar Wolf
Full member
Kiel University
Institute of Biochemistry