Extracellular interaction between hCD98 and the PDZ class II domain of hCASK in intestinal epithelia

J Membr Biol. 2007 Jan;215(1):15-26. doi: 10.1007/s00232-007-9001-8. Epub 2007 Apr 17.

Abstract

The extracellular domain of the glycoprotein-associated integrin hCD98 protrudes into the basolateral extracellular space of the intestine and contains a PDZ class II-binding domain (GLLLRFPYAA, amino acids 520-529). Protein-protein interaction studies in vitro as well as in human colonic sections and Caco2-BBE cells have revealed that hCD98 coimmunoprecipitated with the basolateral membrane-associated guanylate kinase hCASK and that this interaction occurred in a PDZ domain-dependent manner. These novel results, which provide the first evidence for a PDZ domain-dependent interaction between a membrane protein and an extracellular protein, open a new field of investigation related to extracellular signaling in cell biology.

Publication types

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

MeSH terms

  • Caco-2 Cells
  • Fusion Regulatory Protein-1 / metabolism*
  • Guanylate Kinases / metabolism*
  • Humans
  • Intestinal Mucosa / metabolism*
  • Membrane Proteins / metabolism*
  • Protein Structure, Tertiary

Substances

  • Fusion Regulatory Protein-1
  • Membrane Proteins
  • CASK kinases
  • Guanylate Kinases