The PHCCEx domain of Tiam1/2 is a novel protein- and membrane-binding module

• Shin-ichi Terawaki ^[1] ; Ken Kitano ^[1] ; Tomoyuki Mori ^[1] ; Yan Zhai ^[1] ; Yoshiki Higuchi ^[2] ; Norimichi Itoh ^[3] ; Takashi Watanabe ^[3] ; Kozo Kaibuchi ^[3] ; Toshio Hakoshima ^[1]
  1. [1] Nara Institute of Science and Technology

     Nara Institute of Science and Technology

     Japón

     
  2. [2] University of Hyogo

     University of Hyogo

     Chuo-ku, Japón

     
  3. [3] Nagoya University

     Nagoya University

     Naka-ku, Japón

     

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• Localización: EMBO journal: European Molecular Biology Organization, ISSN 0261-4189, Vol. 29, Nº. 1, 2009, págs. 236-250
• Idioma: inglés
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• Resumen

  • Tiam1 and Tiam2 (Tiam1/2) are guanine nucleotide-exchange factors that possess the PH–CC–Ex (pleckstrin homology, coiled coil and extra) region that mediates binding to plasma membranes and signalling proteins in the activation of Rac GTPases. Crystal structures of the PH–CC–Ex regions revealed a single globular domain, PHCCEx domain, comprising a conventional PH subdomain associated with an antiparallel coiled coil of CC subdomain and a novel three-helical globular Ex subdomain. The PH subdomain resembles the β-spectrin PH domain, suggesting non-canonical phosphatidylinositol binding. Mutational and binding studies indicated that CC and Ex subdomains form a positively charged surface for protein binding. We identified two unique acidic sequence motifs in Tiam1/2-interacting proteins for binding to PHCCEx domain, Motif-I in CD44 and ephrinB's and the NMDA receptor, and Motif-II in Par3 and JIP2. Our results suggest the molecular basis by which the Tiam1/2 PHCCEx domain facilitates dual binding to membranes and signalling proteins.