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Time-dependent catalytic activity in aging condensates

Author

Listed:
  • Wei Kang

    (Dalian University of Technology
    Ningbo Institute of Dalian University of Technology)

  • Zhiyue Wu

    (Dalian University of Technology)

  • Xinzhi Huang

    (Kennesaw State University)

  • Hongbin Qi

    (Dalian University of Technology)

  • Jiaxuan Wu

    (Xi’an Jiaotong-Liverpool University)

  • Jiahui Wang

    (Dalian University of Technology)

  • Jing Li

    (New Territories)

  • Sijin Wu

    (Xi’an Jiaotong-Liverpool University)

  • Byung-Ho Kang

    (New Territories)

  • Bo Li

    (Kennesaw State University)

  • Juncai Ma

    (New Territories)

  • Chuang Xue

    (Dalian University of Technology
    Ningbo Institute of Dalian University of Technology)

Abstract

Biomolecular condensates are dynamic cellular compartments that concentrate proteins and enzymes to regulate biochemical reactions in time and space. While these condensates can enhance enzyme activity, how this function changes as condensates age remains poorly understood. Here, we design synthetic catalytic condensates that selectively recruit enzymes to investigate this temporal evolution. We show that catalytic condensates exhibit time-dependent activity: they initially accelerate enzymatic reactions but gradually lose efficiency due to the transition from liquid-like to solid-like states. This aging process, characterized by protein aggregation and loss of selective barriers, impairs enzyme function both in vitro and living cells. We further demonstrate that small molecules which influence aging dynamics can modulate catalytic efficiency of condensates. Our findings show that condensate aging as a key regulator of enzymatic activity and provide crucial insights for designing functional synthetic condensates.

Suggested Citation

  • Wei Kang & Zhiyue Wu & Xinzhi Huang & Hongbin Qi & Jiaxuan Wu & Jiahui Wang & Jing Li & Sijin Wu & Byung-Ho Kang & Bo Li & Juncai Ma & Chuang Xue, 2025. "Time-dependent catalytic activity in aging condensates," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62074-5
    DOI: 10.1038/s41467-025-62074-5
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