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Updated: Jun 26, 2026

Structural Studies of Macromolecules in Solution using Small Angle X-Ray Scattering
Published on: November 5, 2018
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.
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.
Abstract:
Dendritic cells, a sentinel immunity cell lineage, include different cell subsets that express various C-type lectins. For example, epidermal Langerhans cells express langerin, and some dermal dendritic cells express DC-SIGN. Langerin is a crucial component of Birbeck granules, the Langerhans cell hallmark organelle, and may have a preventive role toward HIV, by its internalization into Birbeck granules. Since langerin carbohydrate recognition domain (CRD) is crucial for HIV interaction and Birbeck granule formation, we produced the CRD of human langerin and solved its structure at 1.5 A resolution. On this basis gp120 high-mannose oligosaccharide binding has been evaluated by molecular modeling. Hydrodynamic studies reveal a very elongated shape of recombinant langerin extracellular domain (ECD). A molecular model of the langerin ECD, integrating the CRD structure, has been generated and validated by comparison with hydrodynamic parameters. In parallel, Langerhans cells were isolated from human skin. From their analysis by electron microscopy and the langerin ECD model, an ultrastructural organization is proposed for Birbeck granules. To delineate the role of the different langerin domains in Birbeck granule formation, we generated truncated and mutated langerin constructs. After transfection into a fibroblastic cell line, we highlighted, in accordance with our model, the role of the CRD in the membrane zipping occurring in BG formation as well as some contribution of the cytoplasmic domain. Finally, we have shown that langerin ECD triggering with a specific mAb promotes global rearrangements of LC morphology. Our results open the way to the definition of a new membrane deformation mechanism.
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