Skip to content
DraconiticResearch
Search Sources API
206,698 studies31 sourcesUpdated 43 min ago
PreprintCC BYHAL

Dynamics of phosphofructokinase condensation are regulated by metabolic and redox cues

Abstract

Condensation of phosphofructokinase, the rate-limiting enzyme of glycolysis, into granules has been observed across species and in various stress conditions. However, it remains unclear what mechanisms govern this process. Here, we show that the two subunits of yeast phosphofructokinase, Pfk1 and Pfk2, assemble into granules even in the absence of exogenous stress, challenging the notion that PFK condensation in yeast is restricted to quiescent or stressed cells. While phosphofructokinase granules are predominant in replicatively aged cells, they are independent of cell division and can form before or after cells cease dividing. We further demonstrate that both subunits can co-localise to the same granules and that Pfk2 requires the disordered N-terminus of Pfk1 for assembly. Strikingly, phosphofructokinase granules are largely absent in cells engaged in respiration or lacking respiratory capacity, but their formation is strongly induced during the metabolic transition from fermentation to respiration. This suggests that phosphofructokinase condensation is tightly linked to the metabolic strategy of the cell. Moreover, we find that reactive oxygen species signaling, mediated by superoxide dismutase 1 (Sod1), modulates phosphofructokinase granule formation, as cells deficient in Sod1 exhibit impaired granule assembly. Overall, our results indicate that phosphofructokinase condensation is a dynamic process regulated by metabolic and redox cues.

Related

  1. Glucose-6-phosphate dehydrogenase at the crossroads of redox homeostasis and regulated cell death in erythrocytes
    Nuriye Nuray Ulusu
    Frontiers in PharmacologyPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationCrossrefDOAJ
  2. Metabolic hallmarks of regulated cell death
    Rui Kang, Xin Chen, Guido Kroemer +1
    Cell ResearchPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationPMC
  3. From coarse-grained molecular dynamics simulations to continuum models of biomolecular condensation
    A. Hubman, T. Potisk, F. Merzel
    bioRxivPreprintCC BY-NC-NDFull textBiophysicsbioRxiv
  4. Infrared Laser Heating Reveals a Reversible Phase Transition of Phosphofructokinase 1 in Mammalian Cells
    Morten Mosbach, Sneha Pavanan Kuruvanthara, Lukas Johannknecht +1
    Chemistry (Weinheim an Der Bergstrasse, Germany)Peer-reviewedCC BY 4.0Full textMolecular biology & gene regulationPMC
  5. A Chemically Characterized Polyherbal Extract Selectively Attenuates Chronic Unpredictable Stress-Induced Redox-Sensitive, Inflammatory, and Metabolic Alterations in Female Rats
    Sanja Kovačević, Ljupka Gligorovska, Biljana Bursać +8
    International Journal of Molecular SciencesPeer-reviewedCC BY 4.0Molecular biology & gene regulationCrossref
BibTeX
@misc{reichert2026dynamics,
  title = {{Dynamics of phosphofructokinase condensation are regulated by metabolic and redox cues}},
  author = {Polina Reichert and Snezhana Oliferenko and Fabrice Caudron},
  howpublished = {HAL},
  year = {2026},
  month = jun,
  doi = {10.64898/2026.06.09.731068},
  url = {https://hal.science/hal-05856613v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Dynamics of phosphofructokinase condensation are regulated by metabolic and redox cues
AU  - Polina Reichert
AU  - Snezhana Oliferenko
AU  - Fabrice Caudron
PY  - 2026
DA  - 2026/06/10
PB  - HAL
DO  - 10.64898/2026.06.09.731068
UR  - https://hal.science/hal-05856613v1
AB  - Condensation of phosphofructokinase, the rate-limiting enzyme of glycolysis, into granules has been observed across species and in various stress conditions. However, it remains unclear what mechanisms govern this process. Here, we show that the two subunits of yeast phosphofructokinase, Pfk1 and Pfk2, assemble into granules even in the absence of exogenous stress, challenging the notion that PFK condensation in yeast is restricted to quiescent or stressed cells. While phosphofructokinase granules are predominant in replicatively aged cells, they are independent of cell division and can form before or after cells cease dividing. We further demonstrate that both subunits can co-localise to the same granules and that Pfk2 requires the disordered N-terminus of Pfk1 for assembly. Strikingly, phosphofructokinase granules are largely absent in cells engaged in respiration or lacking respiratory capacity, but their formation is strongly induced during the metabolic transition from fermentation to respiration. This suggests that phosphofructokinase condensation is tightly linked to the metabolic strategy of the cell. Moreover, we find that reactive oxygen species signaling, mediated by superoxide dismutase 1 (Sod1), modulates phosphofructokinase granule formation, as cells deficient in Sod1 exhibit impaired granule assembly. Overall, our results indicate that phosphofructokinase condensation is a dynamic process regulated by metabolic and redox cues.
ER  -