Amyloid-β aggregation is one of the principal causes of amyloidogenic diseases that lead to the loss of neuronal cells and to cognitive impairments. The use of gold nanoparticles treating amyloidogenic diseases is a promising approach, because the chemistry of the gold surface can be tuned in order to have a specific binding, obtaining effective tools to control the aggregation. In this paper, we show, by means of Replica Exchange Solute Tempering Molecular Simulations, how electrostatic interactions drive the absorption of Amyloid-β monomers onto citrates-capped gold nanoparticles. Importantly, upon binding, amyloid monomers show a reduced propensity in forming β-sheets secondary structures that are characteristics of mature amyloid fibril...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Amyloids-β (Aβ) fibrils are involved in several neurodegenerative diseases. In this study, atomistic...
The abnormal self-assembly of the amyloid-β peptide into toxic β-rich aggregates can cause...
Nanoparticles (NPs) are known to exhibit distinct physical and chemical properties compared with the...
Alzheimer’s disease (AD) is characterized by the presence of amyloid-ß (Aß) protein aggregates in th...
Nanoparticles (NPs) are known to exhibit distinct physical and chemical properties compared with the...
Direct exposure or intake of engineered nanoparticles (ENPs) to the human body will trigger a series...
8noGold nanoparticles (AuNPs) proved to be ideal scaffolds to build nanodevices whose performance ca...
Protein aggregation including the formation of dimers and multimers in solution, underlies an array ...
α-Synuclein (α-syn), an aggregation-prone amyloid protein, has been suggested as a potential cause o...
Proteins in proximity of inorganic surfaces and nanoparticles may undergo profound adjustments that ...
Understanding protein amyloidogenesis is an important topic in protein science, fueled by the role o...
Nanoparticles (NPs) have been experimentally found to either promote or inhibit amyloid aggregation ...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Amyloids-β (Aβ) fibrils are involved in several neurodegenerative diseases. In this study, atomistic...
The abnormal self-assembly of the amyloid-β peptide into toxic β-rich aggregates can cause...
Nanoparticles (NPs) are known to exhibit distinct physical and chemical properties compared with the...
Alzheimer’s disease (AD) is characterized by the presence of amyloid-ß (Aß) protein aggregates in th...
Nanoparticles (NPs) are known to exhibit distinct physical and chemical properties compared with the...
Direct exposure or intake of engineered nanoparticles (ENPs) to the human body will trigger a series...
8noGold nanoparticles (AuNPs) proved to be ideal scaffolds to build nanodevices whose performance ca...
Protein aggregation including the formation of dimers and multimers in solution, underlies an array ...
α-Synuclein (α-syn), an aggregation-prone amyloid protein, has been suggested as a potential cause o...
Proteins in proximity of inorganic surfaces and nanoparticles may undergo profound adjustments that ...
Understanding protein amyloidogenesis is an important topic in protein science, fueled by the role o...
Nanoparticles (NPs) have been experimentally found to either promote or inhibit amyloid aggregation ...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...
Nanoparticles have repeatedly been shown to enhance fibril formation when assayed with amyloidogenic...