ENTH/ANTH proteins and clathrin-mediated membrane budding

Valerie Legendre-Guillemin, Sylwia Wasiak, Natasha K. Hussain, Annie Angers, Peter S. McPherson

Research output: Contribution to journalArticlepeer-review


The epsin N-terminal homology (ENTH) domain is an evolutionarily conserved protein module found primarily in proteins that participate in clathrin-mediated endocytosis. Structural analyses and ligand-binding studies have shown that a set of proteins previously designated as harboring an ENTH domain in fact contain a highly similar, yet unique module referred to as an AP180 N-terminal homology (ANTH) domain. ENTH and ANTH (E/ANTH) domains bind both inositol phospholipids and proteins and contribute to the nucleation and formation of clathrin coats on membranes. ENTH domains also function in the development of membrane curvature through lipid remodeling during the formation of clathrin-coated vesicles. E/ANTH-bearing proteins have recently been shown to function with adaptor protein-1 and GGA adaptors at the trans-Golgi network, which suggests that E/ANTH domains are universal components of the machinery for clathrin-mediated membrane budding.

Original languageEnglish (US)
Pages (from-to)9-18
Number of pages10
JournalJournal of cell science
Issue number1
StatePublished - Jan 1 2004


  • ANTH domain
  • Clathrin-coated vesicle
  • ENTH domain
  • Phosphoinositides
  • Trans-Golgi network

ASJC Scopus subject areas

  • Cell Biology


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