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Published on: March 20, 2015
Structural basis for selective recognition of oligosaccharides by DC-SIGN and DC-SIGNR
H Feinberg1, D A Mitchell, K Drickamer
1Department of Structural Biology, University School of Medicine, Stanford, CA 94305, USA.
Dendritic cell specific intracellular adhesion molecule-3 grabbing nonintegrin (DC-SIGN) binds to HIV, promoting infection. Understanding DC-SIGN and DC-SIGNR binding to high-mannose oligosaccharides may lead to new HIV prophylactics.
Area of Science:
- Immunology
- Virology
- Structural Biology
Background:
- Dendritic cell specific intracellular adhesion molecule-3 grabbing nonintegrin (DC-SIGN) is a C-type lectin on dendritic cells that binds ICAM-3, mediating initial T cell interactions.
- DC-SIGN and the related DC-SIGNR receptor bind to oligosaccharides on the human immunodeficiency virus (HIV) envelope, enhancing viral infection of T cells.
Purpose of the Study:
- To elucidate the structural basis of DC-SIGN and DC-SIGNR recognition of oligosaccharides.
- To explore the potential of these interactions for developing novel HIV prophylactics.
Main Methods:
- X-ray crystallography was used to determine the structures of the carbohydrate-recognition domains of DC-SIGN and DC-SIGNR bound to oligosaccharides.
- Binding studies were conducted to assess the selectivity of these receptors for specific oligosaccharides.
Main Results:
- The crystal structures revealed how DC-SIGN and DC-SIGNR bind to specific oligosaccharide structures.
- Binding studies confirmed that these receptors selectively recognize endogenous high-mannose oligosaccharides.
Conclusions:
- DC-SIGN and DC-SIGNR's selective recognition of high-mannose oligosaccharides provides a molecular understanding of their role in HIV infection.
- Targeting these interactions represents a promising new strategy for developing effective HIV prophylactics.
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