Origins of Peptide Selectivity and Phosphoinositide Binding Revealed by Structures of disabled-1 PTB Domain Complexes

Structure. 2003 May;11(5):569-79. doi: 10.1016/s0969-2126(03)00068-6.

Abstract

Formation of the mammalian six-layered neocortex depends on a signaling pathway that involves Reelin, the very low-density lipoprotein receptor, the apolipoprotein E receptor-2 (ApoER2), and the adaptor protein Disabled-1 (Dab1). The 1.5 A crystal structure of a complex between the Dab1 phosphotyrosine binding (PTB) domain and a 14-residue peptide from the ApoER2 tail explains the unusual preference of Dab1 for unphosphorylated tyrosine within the NPxY motif of the peptide. Crystals of the complex soaked with the phosphoinositide PI-4,5P(2) (PI) show that PI binds to conserved basic residues on the PTB domain opposite the peptide binding groove. This finding explains how the Dab1 PTB domain can simultaneously bind PI and the ApoER2 tail. Recruitment of the Dab1 PTB domain to PI-rich regions of the plasma membrane may facilitate association with the Reelin receptor cytoplasmic tails to transduce a critical positional cue to migrating neurons.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Crystallography, X-Ray
  • Humans
  • Molecular Sequence Data
  • Nerve Tissue Proteins / chemistry*
  • Nerve Tissue Proteins / metabolism
  • Peptides / metabolism*
  • Phosphatidylinositols / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary
  • Sequence Alignment

Substances

  • Adaptor Proteins, Signal Transducing
  • DAB1 protein, human
  • Nerve Tissue Proteins
  • Peptides
  • Phosphatidylinositols

Associated data

  • PDB/1NTV
  • PDB/1NU2