Flavonoids with Vicinal Hydroxyl Groups Inhibit Human Calcitonin Amyloid Formation.

Lantz, Richard; Busbee, Brian; Wojcikiewicz, Ewa P.; Du, Deguo

Human calcitonin (hCT) is a 32‐residue peptide hormone that can aggregate into amyloid fibrils and cause cellular toxicity. In this study, we investigated the inhibition effects of a group of polyphenolic molecules on hCT amyloid formation. Our results suggest that the gallate moiety in epigallocatechin‐3‐gallate (EGCG), a well‐recognized amyloid inhibitor, is not critical for its inhibition function in the hCT amyloid formation. Our results demonstrate that flavonoid compounds, such as myricetin, quercetin, and baicalein, that contain vicinal hydroxyl groups on the phenyl ring effectively prevent hCT fibrillization. This structural feature may also be applied to non‐flavonoid polyphenolic inhibitors. Moreover, our results indicate a plausible mechanistic role of these vicinal hydroxyl groups which might include the oxidation to form a quinone and the subsequent covalent linkage with amino acid residues such as lysine or histidine in hCT. This may further disrupt the crucial electrostatic and aromatic interactions involved in the process of hCT amyloid fibril formation. The inhibition activity of the polyphenolic compounds against hCT fibril formation may likely be attributed to a combination of factors such as covalent linkage formation, aromatic stacking, and hydrogen bonding interactions.

CALCITONIN; HYDROXYL group; EPIGALLOCATECHIN gallate; AMYLOID; AMINO acid residues; PEPTIDE hormones; HYDROGEN bonding interactions

Chemistry - A European Journal, 2020, Vol 26, Issue 57, p13063

0947-6539

Academic Journal

10.1002/chem.202002027