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Cellular and Molecular Life Sciences CMLS

, Volume 63, Issue 4, pp 505–514 | Cite as

On the self-association potential of transmembrane tight junction proteins

  • I. E. Blasig†Email author
  • L. Winkler†
  • B. Lassowski
  • S. L. Mueller
  • N. Zuleger
  • E. Krause
  • G. Krause
  • K. Gast
  • M. Kolbe
  • J. Piontek
Research Article

Abstract.

Tight junctions seal intercellular clefts via membrane-related strands, hence, maintaining important organ functions. We investigated the self-association of strand-forming transmembrane tight junction proteins. The regulatory tight junction protein occludin was differently tagged and cotransfected in eucaryotic cells. These occludins colocalized within the plasma membrane of the same cell, coprecipitated and exhibited fluorescence resonance energy transfer. Differently tagged strand-forming claudin-5 also colocalized in the plasma membrane of the same cell and showed fluorescence resonance energy transfer. This demonstrates self-association in intact cells both of occludin and claudin-5 in one plasma membrane. In search of dimerizing regions of occludin, dimerization of its cytosolic C-terminal coiledcoil domain was identified. In claudin-5, the second extracellular loop was detected as a dimer. Since the transmembrane junctional adhesion molecule also is known to dimerize, the assumption that homodimerization of transmembrane tight junction proteins may serve as a common structural feature in tight junction assembly is supported.

Key words.

Occludin claudin-5 tight junction dimerization protein-protein interaction 

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Copyright information

© Birkhäuser Verlag, Basel 2006

Authors and Affiliations

  • I. E. Blasig†
    • 1
    Email author
  • L. Winkler†
    • 1
  • B. Lassowski
    • 1
  • S. L. Mueller
    • 1
  • N. Zuleger
    • 1
  • E. Krause
    • 1
  • G. Krause
    • 1
  • K. Gast
    • 2
  • M. Kolbe
    • 3
  • J. Piontek
    • 1
  1. 1.Forschungsinstitut für Molekulare PharmakologieBerlinGermany
  2. 2.Institute for Biochemistry and BiologyUniversität PotsdamPotsdamGermany
  3. 3.Max-Planck-Institute for Infection BiologyBerlinGermany

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