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Growing and surviving: How proteins regulate the cell cycle

Date:
March 23, 2018
Source:
Martin-Luther-Universität Halle-Wittenberg
Summary:
Cell division is the basis of all life. Even the smallest errors in this complex process can lead to grave diseases like cancer. Certain proteins have to be switched on or off at certain times for everything to go according to plan. Biophysicists and medical biochemists have managed to describe the underlying mechanism of this process.
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Cell division is the basis of all life. Even the smallest errors in this complex process can lead to grave diseases like cancer. Certain proteins have to be switched on or off at certain times for everything to go according to plan. Biophysicists and medical biochemists at Martin Luther University Halle-Wittenberg (MLU) have managed to describe the underlying mechanism of this process. They have figured out how different signaling pathways in the cell change the structure of proteins, thereby driving the cell division cycle in the right direction at the right time. The researchers present their findings in the journal Proceedings of the National Academy of Sciences.

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.


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Materials provided by Martin-Luther-Universität Halle-Wittenberg. Note: Content may be edited for style and length.


Journal Reference:

  1. Amit Kumar, Mohanraj Gopalswamy, Annika Wolf, David J. Brockwell, Mechthild Hatzfeld, Jochen Balbach. Phosphorylation-induced unfolding regulates p19INK4dduring the human cell cycle. Proceedings of the National Academy of Sciences, 2018; 201719774 DOI: 10.1073/pnas.1719774115

Cite This Page:

Martin-Luther-Universität Halle-Wittenberg. "Growing and surviving: How proteins regulate the cell cycle." ScienceDaily. ScienceDaily, 23 March 2018. <www.sciencedaily.com/releases/2018/03/180323104819.htm>.
Martin-Luther-Universität Halle-Wittenberg. (2018, March 23). Growing and surviving: How proteins regulate the cell cycle. ScienceDaily. Retrieved December 3, 2024 from www.sciencedaily.com/releases/2018/03/180323104819.htm
Martin-Luther-Universität Halle-Wittenberg. "Growing and surviving: How proteins regulate the cell cycle." ScienceDaily. www.sciencedaily.com/releases/2018/03/180323104819.htm (accessed December 3, 2024).

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