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1.
Angew Chem Int Ed Engl ; 53(34): 8985-90, 2014 Aug 18.
Artículo en Inglés | MEDLINE | ID: mdl-24985739

RESUMEN

The disruption of Aß homeostasis, which results in the accumulation of neurotoxic amyloids, is the fundamental cause of Alzheimer's disease (AD). Molecular chaperones play a critical role in controlling undesired protein misfolding and maintaining intricate proteostasis in vivo. Inspired by a natural molecular chaperone, an artificial chaperone consisting of mixed-shell polymeric micelles (MSPMs) has been devised with tunable surface properties, serving as a suppressor of AD. Taking advantage of biocompatibility, selectivity toward aberrant proteins, and long blood circulation, these MSPM-based chaperones can maintain Aß homeostasis by a combination of inhibiting Aß fibrillation and facilitating Aß aggregate clearance and simultaneously reducing Aß-mediated neurotoxicity. The balance of hydrophilic/hydrophobic moieties on the surface of MSPMs is important for their enhanced therapeutic effect.


Asunto(s)
Péptidos beta-Amiloides/química , Homeostasis , Micelas , Chaperonas Moleculares/química , Polímeros/química , Dicroismo Circular , Cinética , Microscopía Electrónica de Transmisión , Espectrofotometría Ultravioleta
2.
ACS Appl Mater Interfaces ; 8(6): 3669-78, 2016 Feb 17.
Artículo en Inglés | MEDLINE | ID: mdl-26570996

RESUMEN

Artificial chaperones are of great interest in fighting protein misfolding and aggregation for the protection of protein bioactivity. A comprehensive understanding of the interaction between artificial chaperones and proteins is critical for the effective utilization of these materials in biomedicine. In this work, we fabricated three kinds of artificial chaperones with different surface charges based on mixed-shell polymeric micelles (MSPMs), and investigated their protective effect for lysozymes under thermal stress. It was found that MSPMs with different surface charges showed distinct chaperone-like behavior, and the neutral MSPM with PEG shell and PMEO2MA hydrophobic domain at high temperature is superior to the negatively and positively charged one, because of the excessive electrostatic interactions between the protein and charged MSPMs. The results may benefit to optimize this kind of artificial chaperone with enhanced properties and expand their application in the future.


Asunto(s)
Proteínas Aviares/química , Micelas , Chaperonas Moleculares/química , Muramidasa/química , Polietilenglicoles/química , Replegamiento Proteico , Animales , Pollos , Calor , Humanos , Desnaturalización Proteica
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