Oxidatively-mediated in silico epimerization of a highly amyloidogenic segment in the human calcitonin hormone (hCT15-19)
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
31048244
DOI
10.1016/j.compbiolchem.2019.04.005
PII: S1476-9271(19)30022-2
Knihovny.cz E-resources
- Keywords
- Aggregation, Amyloidosis, DFNKF, Molecular ageing, Oxidative-stress, Peptide,
- MeSH
- Amyloid beta-Peptides chemistry MeSH
- Amyloidogenic Proteins chemistry MeSH
- Models, Chemical MeSH
- Calcitonin chemistry MeSH
- Humans MeSH
- Oxidation-Reduction MeSH
- Peptide Fragments chemistry MeSH
- Protein Structure, Secondary MeSH
- Molecular Dynamics Simulation MeSH
- Stereoisomerism MeSH
- Density Functional Theory MeSH
- Thermodynamics MeSH
- Hydrogen Bonding MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- amyloid beta-protein (1-42) MeSH Browser
- Amyloid beta-Peptides MeSH
- Amyloidogenic Proteins MeSH
- calcitionin(15-19) peptide, human MeSH Browser
- Calcitonin MeSH
- Peptide Fragments MeSH
In order to study the effects of peptide exposure to oxidative attack, we chose a model reaction in which the hydroxyl radical discretely abstracts a hydrogen atom from the α-carbon of each residue of a highly amyloidogenic region in the human calcitonin hormone, hCT15-19. Based on a combined Molecular Mechanics / Quantum Mechanics approach, the extended and folded L- and D-configuration and radical intermediate hCT15-19 peptides were optimized to obtain their compactness, secondary structure and relative thermodynamic data. The results suggest that the epimerization of residues is generally an exergonic process that can explain the cumulative nature of molecular aging. Moreover, the configurational inversion induced conformational changes can cause protein dysfunction. The epimerization of the central residue to the D-configuration induced a hairpin structure in hCT15-19, concomitant with a possible oligomerization of human calcitonin into Aβ(1-42)-like amyloid fibrils present in patients suffering from Alzheimer's disease.
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