Inhibition of FGFR Signaling by Targeting FGF/FGFR Extracellular Interactions: Towards the Comprehension of the Molecular Mechanism through NMR Approaches
Autor: | Katiuscia Pagano, Elisa Longhi, Henriette Molinari, Giulia Taraboletti, Laura Ragona |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: |
Organic Chemistry
General Medicine Receptors Fibroblast Growth Factor Catalysis Computer Science Applications Inorganic Chemistry Fibroblast Growth Factors Adenosine Triphosphate Neoplasms Humans Fibroblast Growth Factor 2 Physical and Theoretical Chemistry Comprehension Molecular Biology Spectroscopy Signal Transduction NMR DOSY fibroblast growth factor rosmarinic acid resveratrol dobesilate allosteric inhibitors |
Zdroj: | International Journal of Molecular Sciences; Volume 23; Issue 18; Pages: 10860 |
ISSN: | 1422-0067 |
DOI: | 10.3390/ijms231810860 |
Popis: | NMR-based approaches play a pivotal role in providing insight into molecular recognition mechanisms, affording the required atomic-level description and enabling the identification of promising inhibitors of protein–protein interactions. The aberrant activation of the fibroblast growth factor 2 (FGF2)/fibroblast growth factor receptor (FGFR) signaling pathway drives several pathologies, including cancer development, metastasis formation, resistance to therapy, angiogenesis-driven pathologies, vascular diseases, and viral infections. Most FGFR inhibitors targeting the intracellular ATP binding pocket of FGFR have adverse effects, such as limited specificity and relevant toxicity. A viable alternative is represented by targeting the FGF/FGFR extracellular interactions. We previously identified a few small-molecule inhibitors acting extracellularly, targeting FGFR or FGF. We have now built a small library of natural and synthetic molecules that potentially act as inhibitors of FGF2/FGFR interactions to improve our understanding of the molecular mechanisms of inhibitory activity. Here, we provide a comparative analysis of the interaction mode of small molecules with the FGF2/FGFR complex and the single protein domains. DOSY and residue-level NMR analysis afforded insights into the capability of the potential inhibitors to destabilize complex formation, highlighting different mechanisms of inhibition of FGF2-induced cell proliferation. |
Databáze: | OpenAIRE |
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