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Force-activated zyxin assemblies coordinate actin nucleation and crosslinking to orchestrate stress fiber repair.

Donovan Y Z PhuaXiaoyu SunGregory M Alushin
Published in: bioRxiv : the preprint server for biology (2024)
As the cytoskeleton sustains cell and tissue forces, it incurs physical damage that must be repaired to maintain mechanical homeostasis. The LIM-domain protein zyxin detects force-induced ruptures in actin-myosin stress fibers, coordinating downstream repair factors to restore stress fiber integrity through unclear mechanisms. Here, we reconstitute stress fiber repair with purified proteins, uncovering detailed links between zyxin's force-regulated binding interactions and cytoskeletal dynamics. In addition to binding individual tensed actin filaments (F-actin), zyxin's LIM domains form force-dependent assemblies that bridge broken filament fragments. Zyxin assemblies engage repair factors through multi-valent interactions, coordinating nucleation of new F-actin by VASP and its crosslinking into aligned bundles by ɑ-actinin. Through these combined activities, stress fiber repair initiates within the cores of micron-scale damage sites in cells, explaining how these F-actin depleted regions are rapidly restored. Thus, zyxin's force-dependent organization of actin repair machinery inherently operates at the network scale to maintain cytoskeletal integrity.
Keyphrases
  • cell migration
  • single molecule
  • stress induced
  • mental health
  • stem cells
  • transcription factor
  • single cell
  • cell proliferation
  • high glucose
  • dna binding
  • network analysis
  • endoplasmic reticulum stress