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  Filament formation by metabolic enzymes is a specific adaptation to an advanced state of cellular starvation.

Petrovska, I., Nüske, E., Munder, M., Kulasegaran, G., Malinovska, L., Kroschwald, S., et al. (2014). Filament formation by metabolic enzymes is a specific adaptation to an advanced state of cellular starvation. eLife, 3: doi: 10.1101/003277.

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 Creators:
Petrovska, Ivana1, Author           
Nüske, Elisabeth1, Author           
Munder, Matthias1, Author           
Kulasegaran, Gayathrie1, Author           
Malinovska, Liliana1, Author           
Kroschwald, Sonja1, Author           
Richter, Doris1, Author           
Fahmy, Karim, Author
Gibson, Kimberley1, Author           
Verbavatz, Jean-Marc1, Author           
Alberti, Simon1, Author           
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1Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Abstract: One of the key questions in biology is how the metabolism of a cell responds to changes in the environment. In budding yeast, starvation causes a drop in intracellular pH, but the functional role of this pH change is not well understood. Here, we show that the enzyme glutamine synthetase (Gln1) forms filaments at low pH and that filament formation leads to enzymatic inactivation. Filament formation by Gln1 is a highly cooperative process, strongly dependent on macromolecular crowding, and involves back-to-back stacking of cylindrical homo-decamers into filaments that associate laterally to form higher order fibrils. Other metabolic enzymes also assemble into filaments at low pH. Hence, we propose that filament formation is a general mechanism to inactivate and store key metabolic enzymes during a state of advanced cellular starvation. These findings have broad implications for understanding the interplay between nutritional stress, the metabolism and the physical organization of a cell.

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 Dates: 2014
 Publication Status: Issued
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 Identifiers: eDoc: 705643
Other: 5724
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Title: eLife
Source Genre: Journal
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Pages: - Volume / Issue: 3 Sequence Number: doi: 10.1101/003277 Start / End Page: - Identifier: -