Structural studies of langerin and Birbeck granule: a macromolecular organization model

Michel Thépaut1, Jenny Valladeau, Alessandra Nurisso

  • 1Laboratoire des Proteines Membranaires, CEA, DSV, Institut de Biologie Structurale (IBS), Grenoble, France.

Biochemistry
|January 30, 2009
PubMed

Insights

Langerin, a C-type lectin on Langerhans cells, is key for Birbeck granule formation and potential HIV prevention. Its carbohydrate recognition domain (CRD) structure and function in membrane zipping were elucidated, revealing a new membrane deformation mechanism.

Area of Science:

  • Immunology
  • Cell Biology
  • Structural Biology

Background:

  • Dendritic cells, including Langerhans cells (LCs), express C-type lectins like langerin.
  • Langerin is vital for Birbeck granules (BG), LC organelles implicated in HIV interaction.
  • The langerin carbohydrate recognition domain (CRD) is critical for BG formation and HIV binding.

Purpose of the Study:

  • To determine the structure of the human langerin CRD.
  • To model the langerin extracellular domain (ECD) and its interaction with HIV gp120.
  • To investigate the role of langerin domains in Birbeck granule formation and LC morphology.

Main Methods:

  • X-ray crystallography to solve the CRD structure.
  • Molecular modeling and hydrodynamic studies for ECD modeling.
  • Electron microscopy and transfection of engineered langerin constructs in fibroblastic cells.

Main Results:

  • The structure of human langerin CRD was solved at 1.5 A resolution.
  • A validated molecular model of langerin ECD was generated, showing an elongated shape.
  • The CRD was shown to be essential for membrane zipping in BG formation, with cytoplasmic domain contribution.

Conclusions:

  • The CRD structure and ECD model provide insights into Birbeck granule ultrastructure.
  • Langerin's CRD plays a key role in membrane zipping during BG formation.
  • Langerin ECD triggering induces LC morphological changes, suggesting a novel membrane deformation mechanism.

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