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| ==Solution NMR structure of the peptide 12530 from medicinal leech Hirudo medicinalis in dodecylphosphocholine micelles== | | ==Solution NMR structure of the peptide 12530 from medicinal leech Hirudo medicinalis in dodecylphosphocholine micelles== |
- | <StructureSection load='6rsm' size='340' side='right'caption='[[6rsm]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | + | <StructureSection load='6rsm' size='340' side='right'caption='[[6rsm]]' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[6rsm]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6RSM OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6RSM FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6rsm]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Hirudo_medicinalis Hirudo medicinalis]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6RSM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6RSM FirstGlance]. <br> |
- | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6rsm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6rsm OCA], [http://pdbe.org/6rsm PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6rsm RCSB], [http://www.ebi.ac.uk/pdbsum/6rsm PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6rsm ProSAT]</span></td></tr> | + | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6rsm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6rsm OCA], [https://pdbe.org/6rsm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6rsm RCSB], [https://www.ebi.ac.uk/pdbsum/6rsm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6rsm ProSAT]</span></td></tr> |
| </table> | | </table> |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
| + | [[Category: Hirudo medicinalis]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Arseniev, A S]] | + | [[Category: Arseniev AS]] |
- | [[Category: Grafskaia, E N]] | + | [[Category: Grafskaia EN]] |
- | [[Category: Lazarev, V N]] | + | [[Category: Lazarev VN]] |
- | [[Category: Nadezhdin, K D]] | + | [[Category: Nadezhdin KD]] |
- | [[Category: Talyzina, I A]] | + | [[Category: Talyzina IA]] |
- | [[Category: Antimicrobial peptide]]
| + | |
- | [[Category: Antimicrobial protein]]
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- | [[Category: Dooecylphosphocholine micelle]]
| + | |
- | [[Category: Genome]]
| + | |
- | [[Category: Hirudo medicinali]]
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- | [[Category: Medicinal leech]]
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- | [[Category: Prediction algorithm]]
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| Structural highlights
Publication Abstract from PubMed
The rise of antibiotic resistance has necessitated the development of alternative strategies for the treatment of infectious diseases. Antimicrobial peptides (AMPs), components of the innate immune response in various organisms, are promising next-generation drugs against bacterial infections. The ability of the medicinal leech Hirudo medicinalis to store blood for months with little change has attracted interest regarding the identification of novel AMPs in this organism. In this study, we employed computational algorithms to the medicinal leech genome assembly to identify amino acid sequences encoding potential AMPs. Then, we synthesized twelve candidate AMPs identified by the algorithms, determined their secondary structures, measured minimal inhibitory concentrations against three bacterial species (Escherichia coli, Bacillus subtilis, and Chlamydia thrachomatis), and assayed cytotoxic and haemolytic activities. Eight of twelve candidate AMPs possessed antimicrobial activity, and only two of them, 3967 (FRIMRILRVLKL) and 536-1 (RWRLVCFLCRRKKV), exhibited inhibition of growth of all tested bacterial species at a minimal inhibitory concentration of 10mumol. Thus, we evidence the utility of the developed computational algorithms for the identification of AMPs with low toxicity and haemolytic activity in the medicinal leech genome assembly.
Medicinal leech antimicrobial peptides lacking toxicity represent a promising alternative strategy to combat antibiotic-resistant pathogens.,Grafskaia EN, Nadezhdin KD, Talyzina IA, Polina NF, Podgorny OV, Pavlova ER, Bashkirov PV, Kharlampieva DD, Bobrovsky PA, Latsis IA, Manuvera VA, Babenko VV, Trukhan VM, Arseniev AS, Klinov DV, Lazarev VN Eur J Med Chem. 2019 Jul 4;180:143-153. doi: 10.1016/j.ejmech.2019.06.080. PMID:31302447[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Grafskaia EN, Nadezhdin KD, Talyzina IA, Polina NF, Podgorny OV, Pavlova ER, Bashkirov PV, Kharlampieva DD, Bobrovsky PA, Latsis IA, Manuvera VA, Babenko VV, Trukhan VM, Arseniev AS, Klinov DV, Lazarev VN. Medicinal leech antimicrobial peptides lacking toxicity represent a promising alternative strategy to combat antibiotic-resistant pathogens. Eur J Med Chem. 2019 Jul 4;180:143-153. doi: 10.1016/j.ejmech.2019.06.080. PMID:31302447 doi:http://dx.doi.org/10.1016/j.ejmech.2019.06.080
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