Interaction of Human β-Defensin 2 (HBD2) with Glycosaminoglycans
| Autor: | Dušan Uhrín, Dominic J. Campopiano, Emily S. Seo, Perdita E. Barran, Bärbel S. Blaum, Thomas Vargues, Malcolm Lyon, Martin De Cecco, Jon A. Deakin |
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| Rok vydání: | 2010 |
| Předmět: |
Spectrometry
Mass Electrospray Ionization Binding Sites Magnetic Resonance Spectroscopy beta-Defensins Sulfates Static Electricity Antimicrobial peptides Oligosaccharides Chemotaxis Heparin Heparan sulfate Biochemistry Dermatan sulfate Chemotaxis Leukocyte chemistry.chemical_compound chemistry medicine Humans Electrophoretic mobility shift assay Chondroitin sulfate Defensin Glycosaminoglycans medicine.drug |
| Zdroj: | Seo, E S, Blaum, B S, Vargues, T, De Cecco, M, Deakin, J A, Lyon, M, Barran, P E, Campopiano, D J & Uhrín, D 2010, ' Interaction of Human beta-Defensin 2 (HBD2) with Glycosaminoglycans ', Biochemistry, vol. 49, no. 49, pp. 10486–10495 . https://doi.org/10.1021/bi1011749 |
| ISSN: | 1520-4995 0006-2960 |
| Popis: | Human β-defensin 2 (HBD2) is a member of the defensin family of antimicrobial peptides that plays important roles in the innate and adaptive immune system of both vertebrates and invertebrates. In addition to their direct bactericidal action, defensins are also involved in chemotaxis and Toll-like receptor activation. In analogy to chemokine/glycosaminoglycan (GAG) interactions, GAG-defensin complexes are likely to play an important role in chemotaxis and in presenting defensins to their receptors. Using a gel mobility shift assay, we found that HBD2 bound to a range of GAGs including heparin/heparan sulfate (HS), dermatan sulfate (DS), and chondroitin sulfate. We used NMR spectroscopy of (15)N-labeled HBD2 to map the binding sites for two GAG model compounds, a heparin/HS pentasaccharide (fondaparinux sodium; FX) and enzymatically prepared DS hexasaccharide (DSdp6). We identified a number of basic amino acids that form a common ligand binding site, which indicated that these interactions are predominantly electrostatic. The dissociation constant of the [DSdp6-HBD2] complex was determined by NMR spectroscopy to be 5 ± 5 μM. Binding of FX could not be quantified because of slow exchange on the NMR chemical shift time scale. FX was found to induce HBD2 dimerization as evidenced by the analysis of diffusion coefficients, (15)N relaxation, and nESI-MS measurements. The formation of FX-bridged HBD2 dimers exhibited features of a cooperative binding mechanism. In contrast, the complex with DSdp6 was found to be mostly monomeric. |
| Databáze: | OpenAIRE |
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