ArticleThe Journal of biological chemistry2025
Nootropic benzothiazoles promote dendritic spine formation by targeting fascin-1.
Article in The Journal of biological chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Fascin in dendritic protrusions is required for synaptic plasticity.The Journal of biological chemistry · 2026Article
- Neuronal Actin Remodeling and Its Role in Higher Nervous Activity.International journal of molecular sciences · 2025Review
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Authors and funding
17 authors.
Funding
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.
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Registered trials
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