4.8 Article

Calponin-homology domain mediated bending of membrane-associated actin filaments

期刊

ELIFE
卷 10, 期 -, 页码 -

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ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.61078

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资金

  1. Wellcome Investigator Award [WT 101885MA]
  2. ERC [671083]
  3. Wellcome-Warwick Quantitative Biomedicine Programme (Wellcome Trust ISSF) [RMRCB0058]
  4. DBT-IISc partnership funds
  5. IISc start-up grant
  6. University of Warwick
  7. A*STAR Research Attachment Programme (ARAP) PhD studentship
  8. Wellcome [208384/Z/17/Z]
  9. European Research Council (ERC) [671083] Funding Source: European Research Council (ERC)
  10. Wellcome Trust [208384/Z/17/Z] Funding Source: Wellcome Trust

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Actin filaments play a central role in biological processes, with different protein bindings and molecular motor interactions driving the actin cytoskeleton to exhibit diverse geometries, including curved structures like rings and cages.
Actin filaments are central to numerous biological processes in all domains of life. Driven by the interplay with molecular motors, actin binding and actin modulating proteins, the actin cytoskeleton exhibits a variety of geometries. This includes structures with a curved geometry such as axon-stabilizing actin rings, actin cages around mitochondria and the cytokinetic actomyosin ring, which are generally assumed to be formed by short linear filaments held together by actin cross-linkers. However, whether individual actin filaments in these structures could be curved and how they may assume a curved geometry remains unknown. Here, we show that 'curly', a region from the IQGAP family of proteins from three different organisms, comprising the actin-binding calponin-homology domain and a C-terminal unstructured domain, stabilizes individual actin filaments in a curved geometry when anchored to lipid membranes. Although F-actin is semi-flexible with a persistence length of similar to 10 mu m, binding of mobile curly within lipid membranes generates actin filament arcs and full rings of high curvature with radii below 1 mm. Higher rates of fully formed actin rings are observed in the presence of the actin-binding coiled-coil protein tropomyosin and when actin is directly polymerized on lipid membranes decorated with curly. Strikingly, curly induced actin filament rings contract upon the addition of muscle myosin II filaments and expression of curly in mammalian cells leads to highly curved actin structures in the cytoskeleton. Taken together, our work identifies a new mechanism to generate highly curved actin filaments, which opens a range of possibilities to control actin filament geometries, that can be used, for example, in designing synthetic cytoskeletal structures.

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