Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 11 min ago
PreprintCC BY-NC-NDbioRxiv

Actin pool controls the scaling of dynamic actin networks

  1. 1CEA Grenoble

Abstract

Scaling is a fundamental property of living systems, allowing cells to match the size of their internal components to their volume. The size and shape of cells depend largely on the actin cytoskeleton, whose dynamic self-assembling structures are central to this adaptation. Yet how they self-assemble in a volume-dependent manner remains unresolved. To address this question, we used a biomimetic system consisting of beads propelled by actin polymerization in microwells of different volumes, which allowed us to work with a limited and defined number of components. This approach enabled the first reconstitution, from purified proteins, of dynamic cytoskeletal structures that adapt to the volume of their environment. The scalability of these structures depends on how strongly they deplete monomers from a shared pool, and tuning the disassembly rate is sufficient to shift their scaling regime. Scaling principles also hold for multiple competing structures, with greater competition imposing stronger constraints on the monomer pool. Together, these results establish a mechanistic framework in which a structure's capacity to adapt is set by how much it draws down shared resources as it grows, a principle that may extend to other intracellular structures that scale with the cells that build them.

Related

  1. Softer when Thicker: a Conserved Scaling Law Governs Actin Cortex Mechanics
    Joseph Vermeil, Anumita Jawahar, Valentin Laplaud +8
    HALPreprintCC BY-NC-NDFull textBiophysicsGeneral physicsHALbioRxiv
  2. Semidilute Polymer Scaling Controls PEG-induced Protein Phase Separation
    M. Ahmad, H. Ouzon-Shubeita, M. Whende +2
    bioRxivPreprintCC BY-NCFull textBiophysicsbioRxiv
  3. Inferring scaling laws of branching networks from their geometry by global optimization
    E. Jessen, D. Schillinger, M. C. Steinbach
    bioRxivPreprintAll rights reservedFull textBiophysicsbioRxiv
  4. Dynamic three-dimensional chromatin remodeling in lung disease: mechanistic principles, pathogenic regulatory networks, and translational challenges
    Tiantian Liu, Songshan Jiang, Jing Wang +1
    Frontiers in cell and developmental biologyPeer-reviewedCC BYFull textGeneral biochemistryEurope PMC
  5. ZBP1 specifically binds pre-formed Z-RNA, limiting its potential pool of nucleic acid ligands compared to ADAR1
    Nucleic acids researchPeer-reviewedCC BYFull textMolecular biology & gene regulationEurope PMC
BibTeX
@misc{cantat2026actin,
  title = {{Actin pool controls the scaling of dynamic actin networks}},
  author = {A. Cantat and C. Guerin and N. Morel and B. Vianay and A. Mogilner and M. Thery and L. Blanchoin and A. Colin},
  howpublished = {bioRxiv},
  year = {2026},
  month = nov,
  doi = {10.64898/2026.11.03.763964},
  url = {https://www.biorxiv.org/content/10.64898/2026.11.03.763964v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - Actin pool controls the scaling of dynamic actin networks
AU  - A. Cantat
AU  - C. Guerin
AU  - N. Morel
AU  - B. Vianay
AU  - A. Mogilner
AU  - M. Thery
AU  - L. Blanchoin
AU  - A. Colin
PY  - 2026
DA  - 2026/11/03
PB  - bioRxiv
DO  - 10.64898/2026.11.03.763964
UR  - https://www.biorxiv.org/content/10.64898/2026.11.03.763964v1
AB  - Scaling is a fundamental property of living systems, allowing cells to match the size of their internal components to their volume. The size and shape of cells depend largely on the actin cytoskeleton, whose dynamic self-assembling structures are central to this adaptation. Yet how they self-assemble in a volume-dependent manner remains unresolved. To address this question, we used a biomimetic system consisting of beads propelled by actin polymerization in microwells of different volumes, which allowed us to work with a limited and defined number of components. This approach enabled the first reconstitution, from purified proteins, of dynamic cytoskeletal structures that adapt to the volume of their environment. The scalability of these structures depends on how strongly they deplete monomers from a shared pool, and tuning the disassembly rate is sufficient to shift their scaling regime. Scaling principles also hold for multiple competing structures, with greater competition imposing stronger constraints on the monomer pool. Together, these results establish a mechanistic framework in which a structure's capacity to adapt is set by how much it draws down shared resources as it grows, a principle that may extend to other intracellular structures that scale with the cells that build them.
ER  -