2LXO
Identification of the Structural Traits Mediating the Antimicrobial Activity of a Chimeric Peptide of HBD2 and HBD3
Summary for 2LXO
| Entry DOI | 10.2210/pdb2lxo/pdb |
| NMR Information | BMRB: 18684 |
| Descriptor | Chimeric Peptide (1 entity in total) |
| Functional Keywords | antimicrobial peptide, designer peptide, de novo protein, antimicrobial protein |
| Biological source | synthetic construct |
| Total number of polymer chains | 1 |
| Total formula weight | 4982.06 |
| Authors | Spudy, B.,Soennichsen, F.D.,Waetzig, G.H.,Grotzinger, J.,Jung, S. (deposition date: 2012-08-30, release date: 2013-08-14, Last modification date: 2024-11-06) |
| Primary citation | Spudy, B.,Sonnichsen, F.D.,Waetzig, G.H.,Grotzinger, J.,Jung, S. Identification of structural traits that increase the antimicrobial activity of a chimeric peptide of human beta-defensins 2 and 3. Biochem.Biophys.Res.Commun., 427:207-211, 2012 Cited by PubMed Abstract: Antimicrobial peptides participate in the first line of defence of many organisms against pathogens. In humans, the family of β-defensins plays a pivotal role in innate immunity. Two human β-defensins, β-defensin-2 and -3 (HBD2 and HBD3), show substantial sequence identity and structural similarity. However, HBD3 kills Staphylococcus (S.) aureus with a 4- to 8-fold higher efficiency compared to HBD2, whereas their activities against Escherichia (E.) coli are very similar. The generation of six HBD2/HBD3-chimeric molecules led to the identification of distinct molecular regions which mediate their divergent killing properties. One of the chimeras (chimera C3) killed both E. coli and S. aureus with an even higher efficacy compared to the wild-type molecules. Due to the broad spectrum of its antimicrobial activity against many human multidrug-resistant pathogens, this HBD2/HBD3-chimeric peptide represents a promising candidate for a new class of antibiotics. In order to investigate the structural basis of its exceptional antimicrobial activity, the peptide's tertiary structure was determined by NMR spectroscopy, which allowed its direct comparison to the published structures of HBD2 and HBD3 and the identification of the activity-increasing molecular features. PubMed: 22995312DOI: 10.1016/j.bbrc.2012.09.052 PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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