Publication | Closed Access
Photoexcited Porphyrins as a Strong Suppressor of β‐Amyloid Aggregation and Synaptic Toxicity
15
Citations
17
References
2015
Year
β‐Amyloid AggregationDrosophila Ad ModelPeptide ScienceSynaptic SignalingSocial SciencesAlzheimer's Diseaseβ‐Sheet‐rich Amyloid AggregatesPhototoxicityAbnormal AssemblyDegenerative PathologyProtein MisfoldingBioimagingPhotoexcited PorphyrinsBiophysicsMolecular NeuroscienceBiochemistryPhotochemistryMechanistic PhotochemistryNeurodegenerative DiseasesSynaptic ToxicityCellular NeuroscienceMedicineSmall Molecules
Abstract The abnormal assembly of β‐amyloid (Aβ) peptides into neurotoxic, β‐sheet‐rich amyloid aggregates is a major pathological hallmark of Alzheimer’s disease (AD). Light‐induced photosensitizing molecules can regulate Aβ amyloidogenesis. Multiple photochemical analyses using circular dichroism, atomic force microscopy, dot blot, and native gel electrophoresis verified that photoactivated meso ‐tetra(4‐sulfonatophenyl)porphyrin (TPPS with M=2H + , Zn 2+ , Cu 2+ , Mn 2+ ) successfully inhibits Aβ aggregation in vitro. Furthermore, Aβ toxicity was relieved in the photoexcited‐TPPS‐treated Drosophila AD model. TPPS suppresses neural cell death, synaptic toxicity, and behavioral defects in the Drosophila AD model under blue light illumination. Behavioral phenotypes, including larval locomotion defect and short lifespan caused by Aβ overexpression, were also rescued by blue light‐excited TPPS.
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