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In Silico Analysis of Nanoplastics’ and β-amyloid Fibrils’ Interactions
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Researchers used coarse-grained molecular dynamics simulations to study nanoplastic interactions with beta-amyloid fibrils, finding that nanoplastics can influence amyloid aggregation and potentially play a role in neurodegenerative disease pathways.
Plastic pollution has become a global environmental threat, which leads to an increasing concern over the consequences of plastic exposition on global health. Plastic nanoparticles have been shown to influence the folding of proteins and influence the formation of aberrant amyloid proteins, therefore potentially triggering the development of systemic and local amyloidosis. This work aims to study the interaction between nanoplastics and β-amyloid fibrils to better understand the potential role of nanoplastics in the outbreak of neurodegenerative disorders. Using microsecond-long coarse-grained molecular dynamics simulations, we investigated the interactions between neutral and charged nanoparticles made of the most common plastic materials (i.e., polyethylene, polypropylene, and polystyrene) and β-amyloid fibrils. We observe that the occurrence of contacts, region of amyloid fibril involved, and specific amino acids mediating the interaction depend on the type and charge of the nanoparticles.
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Exploring the Interaction of Human α-Synuclein with Polyethylene Nanoplastics: Insights from Computational Modeling and Experimental Corroboration
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Researchers used computer simulations and lab experiments to study how polyethylene nanoplastics interact with alpha-synuclein, a brain protein linked to neurodegenerative conditions. They found that nanoplastics caused the protein to change its shape and form a compact structure that interacts more strongly with itself, potentially promoting clumping. The study suggests a possible mechanism by which nanoplastics could influence protein behavior in the brain, though the health implications remain to be determined.
Evidence for Protein Misfolding in the Presence of Nanoplastics
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Researchers used molecular dynamics simulations to demonstrate that nanoplastic particles can induce protein misfolding in biological systems. The study represents an early model-based investigation of how nanoplastics may interfere with protein structure and function at the molecular level.
The Effect of Polyethylene Terephthalate Nanoplastics on Amyloid-β Peptide Fibrillation
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Researchers investigated whether PET nanoplastics (50 nm and 140 nm) affect the fibrillation of amyloid-beta peptides associated with Alzheimer's disease pathology. PET nanoplastics at concentrations of 10–100 ppm influenced Aβ aggregation kinetics in a size- and concentration-dependent manner, adding to evidence that nanoplastics reaching the brain may modulate neurodegenerative protein aggregation.
Microplastics and Nanoplastics as Potential Contributors to Neurodegenerative Disease: Mechanistic Links to Dementia, Parkinson's Disease, Epilepsy, and Emerging Therapeutic Opportunities
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Researchers reviewed emerging evidence that micro- and nanoplastics may contribute to neurodegeneration by promoting neuroinflammation, oxidative stress, blood-brain barrier disruption, and direct interactions with aggregation-prone proteins like amyloid-β and α-synuclein, proposing that pre-existing neurological disease may increase susceptibility to particulate accumulation in brain tissue.
Evidence for protein misfolding in the presence of nanoplastics
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Computer simulations suggest that nanoplastics — tiny plastic particles under 5 nanometers — can cause proteins to misfold when they bind together. Misfolded proteins are linked to diseases like Alzheimer's, making this an early warning that nanoplastics may pose risks at the molecular level in living cells.
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