Discovery of Isobavachin, a natural flavonoid, as an Apolipoprotein E4 (ApoE4) structure corrector for Alzheimer's disease
Sachin P. PatiliD, Bella R. Kuehn, Christina McCullough, Dean Bates, Hadil Hazim, Mamadou Diallo, Naomie Francois
Abstract
Alzheimers disease (AD) is a progressive neurodegenerative disease characterized by extensive neurodegeneration and consequent severe memory loss. Apolipoprotein E4 (ApoE4) is the strongest genetic risk factor for AD, with its pathological effects linked to structural instability and altered interactions with lipids and other important disease proteins including amyloid beta (A{beta}) and tau ({tau}). Therefore, correcting and stabilizing the ApoE4 structure has emerged as a promising therapeutic strategy for mitigating its detrimental effects. In this study, we investigated naturally occurring bioavailable flavonoids as ApoE4 stabilizers, focusing on their potential to modulate ApoE4 structure and function. Comprehensive investigation of a focused database using our integrated computational and experimental screening protocol led to the identification of Isobavachin as a potential corrector and stabilizer of ApoE4 structure. In addition, a few other bioavailable flavonoids with similar stabilizing properties were identified, albeit to a much lesser extent as compared to Isobavachin. The findings support the therapeutic potential of flavonoids as ApoE4 modulators and highlight Isobavachin as a lead candidate for further preclinical evaluation. These results provide new insights into the pharmacological targeting of ApoE4 and open avenues for the development of flavonoid-based, ApoE-directed therapies for AD.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 9
- FWCI
- 5.75
- Field percentile
- top 4%
- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Imipramine and olanzapine block apoE4-catalyzed polymerization of Aβ and show evidence of improving Alzheimer's disease cognition
Noah R. Johnson, Athena C.-J. Wang, … Huntington Potter·bioRxiv·Mar 28, 2021
- Apolipoprotein E4 disrupts the neuroprotective action of sortilin in neuronal lipid metabolism and endocannabinoid signaling
Antonino Asaro, Anne‐Sophie Carlo‐Spiewok, … Thomas E. Willnow·Alzheimer s & DementiaPeer-reviewed·Jun 25, 2020
- Apolipoprotein E4 has extensive conformational heterogeneity in lipid free and bound forms
M. D. Stuchell-Brereton, M. I. Zimmerman, … A. Soranno·bioRxiv·Feb 2, 2022
- ApoE4 disrupts interaction of sortilin with fatty acid-binding protein 7 essential to promote lipid signaling
A. Asaro, R. Sinha, … T. Willnow·bioRxiv·May 20, 2021
- In Silico Design of APOE ε4 Interaction Inhibitor Peptides for Alzheimer's Disease
Jaeho Ji, Eunjeong Han, … Hyunsoo Kim·bioRxiv·Sep 3, 2025
- NHE6-Depletion Corrects ApoE4-Mediated Synaptic Impairments and Reduces Amyloid Plaque Load
Theresa Pohlkamp, Xunde Xian, … Joachim Herz·eLifePeer-reviewed·Oct 7, 2021