Structural basis of human VANGL-PRICKLE interaction

Nat Commun. 2025 Jan 3;16(1):132. doi: 10.1038/s41467-024-55396-3.

Abstract

Planar cell polarity (PCP) is an evolutionarily conserved process for development and morphogenesis in metazoans. The well-organized polarity pattern in cells is established by the asymmetric distribution of two core protein complexes on opposite sides of the cell membrane. The Van Gogh-like (VANGL)-PRICKLE (PK) pair is one of these two key regulators; however, their structural information and detailed functions have been unclear. Here, we present five cryo-electron microscopy structures of human VANGL1, VANGL2, and their complexes with PK1 at resolutions of 2.2-3.0 Å. Through biochemical and cell imaging experiments, we decipher the molecular details of the VANGL-PK interaction. Furthermore, we reveal that PK1 can target VANGL-containing intracellular vesicles to the peripheral cell membrane. These findings provide a solid foundation to understand the explicit interaction between VANGL and PK while opening new avenues for subsequent studies of the PCP pathway.

MeSH terms

  • Carrier Proteins / chemistry
  • Carrier Proteins / metabolism
  • Cell Membrane / metabolism
  • Cell Polarity
  • Cryoelectron Microscopy*
  • HEK293 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins* / chemistry
  • Membrane Proteins* / metabolism
  • Membrane Proteins* / ultrastructure
  • Models, Molecular
  • Protein Binding

Substances

  • Membrane Proteins
  • VANGL2 protein, human
  • VANGL1 protein, human
  • Carrier Proteins
  • Intracellular Signaling Peptides and Proteins