The cell cycle is an extremely complex and precisely defined process. „The parent cell has to double its existing components and then divide into to daughter cells. In order to do this, numerous genes have to be switched on and off at very specific times,“ says biophysicist Professor Jochen Balbach from MLU. The cell cycle is sub-divided into various phases. These are controlled by what are known as inhibitors proteins, also called CDK inhibitors. Like a red traffic light, these proteins block transition to the next phase until the cell gives the relevant start signal. The signal to start the next phase of the cell cycle comes from a special enzyme group, the kinases. „Previously we only knew that the kinases passed on the signal by adding a phosphate group onto the CDK inhibitors. There was no knowledge, however, of which kinases do this and the underlying molecular mechanism for this,“ continues Balbach.
Together with the working group led by Professor Mechthild Hatzfeld from the Pathobiochemistry Section of the Medical Faculty of MLU, the researchers have now been able to describe this signaling pathway for the first time. They combined high-resolution magnetic resonance spectroscopy data with methods from cell biology. This meant that the researchers were able to explain the mechanism first in test tubes and then directly in cells. The researchers found that the kinases change the structure of the inhibitor proteins by unfolding them. This process disables the original function of the inhibitor proteins and releases a further blocked kinase that gives the signal for the cell cycle to continue. This local unfolding also triggers the degradation of the inhibitor in the cell, determining the direction in which the progression occurs. The researchers from Halle assume that this mechanism preserved by evolution is the basis of many cellular signal pathways.
About the publication:
Amit Kumar, Mohanraj Gopalswamy, Annika Wolf, David J. Brockwell, Mechthild Hatzfeld, Jochen Balbach: Phosphorylation-induced unfolding regulates p19INK4d during the human cell cycle. Proc. Nat. Acad. Sci. USA (2018). doi: 10.1073/pnas.1719774115