The C2 domains of granuphilin are high-affinity sensors for plasma membrane lipids

Chem Phys Lipids. 2014 Sep:182:29-37. doi: 10.1016/j.chemphyslip.2013.10.009. Epub 2013 Nov 1.

Abstract

Membrane-targeting proteins are crucial components of many cell signaling pathways, including the secretion of insulin. Granuphilin, also known as synaptotagmin-like protein 4, functions in tethering secretory vesicles to the plasma membrane prior to exocytosis. Granuphilin docks to insulin secretory vesicles through interaction of its N-terminal domain with vesicular Rab proteins; however, the mechanisms of granuphilin plasma membrane targeting and release are less clear. Granuphilin contains two C2 domains, C2A and C2B, that interact with the plasma membrane lipid phosphatidylinositol-(4,5)-bisphosphate [PI(4,5)P2]. The goal of this study was to determine membrane-binding mechanisms, affinities, and kinetics of both granuphilin C2 domains using fluorescence spectroscopic techniques. Results indicate that both C2A and C2B bind anionic lipids in a Ca(2+)-independent manner. The C2A domain binds liposomes containing a physiological mixture of lipids including 2% PI(4,5)P2 or PI(3,4,5)P3 with high affinity (apparent K(d, PIPx) of 2-5 nM), and binds nonspecifically with moderate affinity to anionic liposomes lacking phosphatidylinositol phosphate (PIPx) lipids. The C2B domain binds with sub-micromolar affinity to liposomes containing PI(4,5)P2 but does not have a measurable affinity for background anionic lipids. Both domains can be competed away from their target lipids by the soluble PIPx analog inositol-(1,2,3,4,5,6)-hexakisphosphate (IP6), which is a positive regulator of insulin secretion. Potential roles of these interactions in the docking and release of granuphilin from the plasma membrane are discussed.

Keywords: Inositol polyphosphate signaling; Insulin secretion; Phosphatidylinositol-(4,5)-bisphosphate; Protein–lipid interaction; Secretory granule docking; Slp4.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding, Competitive
  • Cell Membrane / metabolism*
  • Humans
  • Insulin / metabolism
  • Insulin Secretion
  • Kinetics
  • Membrane Lipids / metabolism*
  • Models, Molecular
  • Phosphatidylinositol Phosphates / metabolism
  • Phytic Acid / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • Vesicular Transport Proteins / chemistry*
  • Vesicular Transport Proteins / metabolism*

Substances

  • Insulin
  • Membrane Lipids
  • Phosphatidylinositol Phosphates
  • SYTL4 protein, human
  • Vesicular Transport Proteins
  • phosphatidylinositol 3,4,5-triphosphate
  • Phytic Acid