Molecular mechanisms of membrane deformation by I-BAR domain proteins

Curr Biol. 2009 Jan 27;19(2):95-107. doi: 10.1016/j.cub.2008.12.029. Epub 2009 Jan 15.

Abstract

Background: Generation of membrane curvature is critical for the formation of plasma membrane protrusions and invaginations and for shaping intracellular organelles. Among the central regulators of membrane dynamics are the BAR superfamily domains, which deform membranes into tubular structures. In contrast to the relatively well characterized BAR and F-BAR domains that promote the formation of plasma membrane invaginations, I-BAR domains induce plasma membrane protrusions through a poorly understood mechanism.

Results: We show that I-BAR domains induce strong PI(4,5)P(2) clustering upon membrane binding, bend the membrane through electrostatic interactions, and remain dynamically associated with the inner leaflet of membrane tubules. Thus, I-BAR domains induce the formation of dynamic membrane protrusions to the opposite direction than do BAR and F-BAR domains. Strikingly, comparison of different I-BAR domains revealed that they deform PI(4,5)P(2)-rich membranes through distinct mechanisms. IRSp53 and IRTKS I-BARs bind membranes mainly through electrostatic interactions, whereas MIM and ABBA I-BARs additionally insert an amphipathic helix into the membrane bilayer, resulting in larger tubule diameter in vitro and more efficient filopodia formation in vivo. Furthermore, FRAP analysis revealed that whereas the mammalian I-BAR domains display dynamic association with filopodia, the C. elegans I-BAR domain forms relatively stable structures inside the plasma membrane protrusions.

Conclusions: These data define I-BAR domain as a functional member of the BAR domain superfamily and unravel the mechanisms by which I-BAR domains deform membranes to induce filopodia in cells. Furthermore, our work reveals unexpected divergence in the mechanisms by which evolutionarily distinct groups of I-BAR domains interact with PI(4,5)P(2)-rich membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caenorhabditis elegans / cytology
  • Caenorhabditis elegans / metabolism
  • Cell Line
  • Cell Membrane* / chemistry
  • Cell Membrane* / metabolism
  • Cell Membrane* / ultrastructure
  • Fluorescence Recovery After Photobleaching
  • Humans
  • Lipid Bilayers / chemistry
  • Lipid Bilayers / metabolism
  • Membrane Proteins* / chemistry
  • Membrane Proteins* / metabolism
  • Mice
  • Models, Molecular
  • Phosphatidylinositol 4,5-Diphosphate / metabolism
  • Protein Conformation*
  • Protein Structure, Tertiary
  • Pseudopodia / metabolism
  • Pseudopodia / ultrastructure
  • Static Electricity

Substances

  • Lipid Bilayers
  • Membrane Proteins
  • Phosphatidylinositol 4,5-Diphosphate