Direktorin der Abteilung

Foto: Peter Barta © BMC/STJUDE

Brenda Schulman

Foto: Peter Barta © BMC/STJUDE

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Forschungsabteilung "Molekulare Maschinen und Signalwege" (Brenda Schulman)

Dynamik zwischen geschlossener und offener Konfiguration von APC/C<sup>CDC20</sup>-MCC gezeigt anhand einer Morphing ECM Abbildung Bild vergrößern
Dynamik zwischen geschlossener und offener Konfiguration von APC/CCDC20-MCC gezeigt anhand einer Morphing ECM Abbildung

A major form of regulation involves protein and membrane remodelling by their linkage to the small protein ubiquitin, or to structurally-related ubiquitin-like proteins (UBLs).  Ubiquitin and UBLs control timing, subcellular location, assembly, conformation, and activity of thousands of different human proteins and macromolecules.  Moreover, defects in ubiquitin and UBL pathways are associated with numerous diseases including cancers, neurodegenerative disorders, and viral infections.  The group of Brenda Schulman investigates how this regulation is achieved by conformationally dynamic, multiprotein assemblies called “molecular machines”.

Schulman’s group has shown that flexible molecular machines are transiently harnessed into specific conformations by different regulatory factors, which specify distinct activities.  Recent work on one such molecular machine, the Anaphase-promoting complex/Cyclosome, or “APC/C”, which is a master regulator of cell division, is shown in the movie.  Schulman’s team, along with collaborators Jan-Michael Peters (IMP, Vienna) and Holger Stark (MPI Biophysical Chemistry, Göttingen), used cryo electron microscopy and other methods to visualize the different assemblies formed by APC/C and its collaborating activators, inhibitors, substrates, and E2 enzymes that regulate ubiquitylation to promote accurate cell division.

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