Cripto-1 acts as a molecular bridge linking nodal to ALK4 via distinct structural domains

Protein Sci. 2025 Feb;34(2):e70034. doi: 10.1002/pro.70034.

Abstract

The TGF-β family ligand Nodal is an essential regulator of embryonic development, orchestrating key processes such as germ layer specification and body axis formation through activation of SMAD2/3-mediated signaling. Significantly, this activation requires the co-receptor Cripto-1. However, despite their essential roles in embryogenesis, the molecular mechanism through which Cripto-1 enables Nodal to activate the SMAD2/3 pathway has remained elusive. Intriguingly, Cripto-1 also has been shown to antagonize other TGF-β family ligands, raising questions about its diverse functions. To clarify how Cripto-1 modulates TGF-β signaling, we integrated AlphaFold3 modeling, surface plasmon resonance (SPR)-based protein-protein interaction analysis, domain-specific anti-Cripto-1 antibodies, and functional studies in NTERA-2 cells. In contrast to canonical TGF-β signaling, where ligands bridge type I and type II receptors for activation, Nodal, bound to the type II receptor, utilizes Cripto-1 to recruit the type I receptor ALK4, forming a unique ternary complex for SMAD2/3 activation. Our molecular characterization of Cripto-1-mediated Nodal signaling clarifies the unique role of this enigmatic co-receptor and advances our understanding of signaling regulation within the TGF-β family. These insights have potential implications for both developmental biology and cancer research.

Keywords: ALK4; AlphaFold; Cripto‐1; EGF‐CFC proteins; co‐receptor; molecular modeling; nodal; protein–protein interaction; signaling transduction; transforming growth factor beta (TGF‐β).

MeSH terms

  • Activin Receptors, Type I* / chemistry
  • Activin Receptors, Type I* / genetics
  • Activin Receptors, Type I* / metabolism
  • Activin Receptors, Type II / chemistry
  • Activin Receptors, Type II / genetics
  • Activin Receptors, Type II / metabolism
  • GPI-Linked Proteins* / chemistry
  • GPI-Linked Proteins* / genetics
  • GPI-Linked Proteins* / metabolism
  • Humans
  • Intercellular Signaling Peptides and Proteins* / chemistry
  • Intercellular Signaling Peptides and Proteins* / genetics
  • Intercellular Signaling Peptides and Proteins* / metabolism
  • Neoplasm Proteins* / chemistry
  • Neoplasm Proteins* / genetics
  • Neoplasm Proteins* / metabolism
  • Nodal Protein* / chemistry
  • Nodal Protein* / genetics
  • Nodal Protein* / metabolism
  • Protein Binding
  • Protein Domains
  • Signal Transduction
  • Smad2 Protein / chemistry
  • Smad2 Protein / genetics
  • Smad2 Protein / metabolism

Substances

  • TDGF1 protein, human
  • Nodal Protein
  • GPI-Linked Proteins
  • Activin Receptors, Type I
  • Intercellular Signaling Peptides and Proteins
  • Neoplasm Proteins
  • ACVR1B protein, human
  • NODAL protein, human
  • Activin Receptors, Type II
  • Smad2 Protein