Regulation of Aggregation of Self-Associated Peptides, Including N-Terminal Fragments of the Alzheimer's β-Amyloid Peptide, by Nitro Derivatives of Azoloazine.

Autor: Mirgorodskaya, O. A., Kozmin, Y. P., Protasov, A. D., Toropygin, I. Y., Oleinikov, V. A.
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Zdroj: Russian Journal of Bioorganic Chemistry; Nov2018, Vol. 44 Issue 6, p665-675, 11p
Abstrakt: The potential of the nitro compounds of the azoloazine class as regulators of aggregation of natural self-associating peptides was demonstrated by the example of fragments of the Alzheimer β-amyloid peptide and the melittin cytolytic peptide from bee venom. Depending on the type of an azoloazine derivative, association of a peptide into insoluble aggregates either occurred or was suppressed up to the peptide aggregates dissolution. The sites and stoichiometry of the azoloazine binding to the examined peptides are determined in the associates. These effects were explained by a unique ability of the azoloazine nitro derivatives to dissociate in aqueous solutions with the formation of a stable aromatic anion with electrostatic affinity to basic amino acid residues of the peptide molecules. This property of nitroazoloazines was used for a test of their ability to regulate the aggregation processes. Therefore, the nitro derivatives of azoloazines are promising inducers or inhibitors of the aggregation of the Alzheimer β-amyloid peptide and, possibly, other peptides which can form amyloid deposits. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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