Binding mechanism and biological effects of flavone DYRK1A inhibitors for the design of new antidiabetics

• Published in: Scientific reports 2023-10, Vol.13 (1), p.18114-18114, Article 18114
• Main Authors: Pustelny, Katarzyna, Grygier, Przemyslaw, Barzowska, Agata, Pucelik, Barbara, Matsuda, Alex, Mrowiec, Krzysztof, Slugocka, Emilia, Popowicz, Grzegorz M., Dubin, Grzegorz, Czarna, Anna
• Format: Article
• Language: English
• Subjects: 631/154; 631/45; 631/535; 692/4017; 692/699; Alzheimer's disease; Antidiabetics; Beta cells; Biological effects; Cell proliferation; Diabetes; Diabetes mellitus; Down's syndrome; Flavones; Humanities and Social Sciences; Inhibitors; Insulin secretion; multidisciplinary; Neurodegenerative diseases; Science; Science (multidisciplinary); Transforming growth factor-b
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-44810-3

The selective inhibition of kinases from the diabetic kinome is known to promote the regeneration of beta cells and provide an opportunity for the curative treatment of diabetes. The effect can be achieved by carefully tailoring the selectivity of inhibitor toward a particular kinase, especially DYRK1A, previously associated with Down syndrome and Alzheimer's disease. Recently DYRK1A inhibition has been shown to promote both insulin secretion and beta cells proliferation. Here, we show that commonly available flavones are effective inhibitors of DYRK1A. The observed biochemical activity of flavone compounds is confirmed by crystal structures solved at 2.06 Å and 2.32 Å resolution, deciphering the way inhibitors bind in the ATP-binding pocket of the kinase, which is driven by the arrangement of hydroxyl moieties. We also demonstrate antidiabetic properties of these biomolecules and prove that they could be further improved by therapy combined with TGF-β inhibitors. Our data will allow future structure-based optimization of the presented scaffolds toward potent, bioavailable and selective anti-diabetic drugs.