Nootropic benzothiazoles promote dendritic spine formation by targeting fascin-1

Identifying new drug targets to enhance memory and learning is essential for treating neurodegenerative diseases, such as Alzheimer's disease. We previously showed that benzothiazole amphiphiles can improve memory and learning by increasing dendritic spine and synaptic density in both WT mice and in a transgenic Alzheimer's model mice. The cellular target for this class of compounds, however, was unknown. Using a photoaffinity-labeling approach, we identify fascin-1 as the major protein target in neurons for these compounds. These compounds enhance spine density by directly modulating actin dynamics, increasing the capability of fascin-1 to bundle actin filaments. Molecular docking and structure-guided mutagenesis studies reveal a distinct binding site on fascin-1, differing in both location and function from previously reported fascin-1-targeting molecules, opening exciting new avenues for selectively tuning fascin-1 activity in the brain.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-08-08
DOI
https://doi.org/10.1016/j.jbc.2025.110572
Citations
1
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
1.63

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article

Nootropic benzothiazoles promote dendritic spine formation by targeting fascin-1

Geoffray Leriche, Kyle R. Berg, Kevin Carlo Abril Sibucao, Gentry N. Patrick et al.
1 citations
Journal of Biological Chemistry
Advanced Fluorescence Microscopy Techniques
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article

Nootropic benzothiazoles promote dendritic spine formation by targeting fascin-1

Geoffray Leriche, Kyle R. Berg, Kevin Carlo Abril Sibucao, Gentry N. Patrick, Christian Seitz, Lara E. Dozier, Jerry Yang, Jacob M. Wozniak, Zied Gaieb, Rommie Elizabeth Amaro, Saptarshi Sinha, Aashish Shivkumar, David J. Gonzalez, Pradipta Ghosh, Hyun‐Hee Park, Hyang-Sook Hoe, C. Espinoza
article en
1 citations

Abstract

Identifying new drug targets to enhance memory and learning is essential for treating neurodegenerative diseases, such as Alzheimer's disease. We previously showed that benzothiazole amphiphiles can improve memory and learning by increasing dendritic spine and synaptic density in both WT mice and in a transgenic Alzheimer's model mice. The cellular target for this class of compounds, however, was unknown. Using a photoaffinity-labeling approach, we identify fascin-1 as the major protein target in neurons for these compounds. These compounds enhance spine density by directly modulating actin dynamics, increasing the capability of fascin-1 to bundle actin filaments. Molecular docking and structure-guided mutagenesis studies reveal a distinct binding site on fascin-1, differing in both location and function from previously reported fascin-1-targeting molecules, opening exciting new avenues for selectively tuning fascin-1 activity in the brain.

Journal of Biological ChemistryVol. 301(9)
University of California San Diego (US), Korea Brain Research Institute (KR), University of Montana (US)
National Science Foundation, National Institutes of Health, University of California, San Diego, Army Research Office
Good health and well-being
Openalex Percentile: Top 13%
Advanced Fluorescence Microscopy Techniques
1.63
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