Your browser doesn't support javascript.
loading
Mixed Phospholipid Vesicles Catalytically Inhibit and Reverse Amyloid Fibril Formation.
Chaparro Sosa, Andres F; de Oliveira da Silva, Sabrina Matos; Morgan, Garry P; Schwartz, Daniel K; Kaar, Joel L.
Afiliação
  • Chaparro Sosa AF; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States.
  • de Oliveira da Silva SM; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States.
  • Morgan GP; Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado 80309, United States.
  • Schwartz DK; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States.
  • Kaar JL; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States.
J Phys Chem Lett ; 11(17): 7417-7422, 2020 Sep 03.
Article em En | MEDLINE | ID: mdl-32803986
While many approaches to reduce fibrillation of amyloid-ß (Aß) have been aimed at slowing fibril formation, the degradation of fibrils remains challenging. We provide insight into fibril degradation as well as the inhibition of fiber formation by lipid vesicles composed of 1,2-dioleoyl-sn-glycero-3-phosphocholine and 1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol). In the presence of vesicles with the optimal lipid composition, fibril formation was inhibited up to 76%. Additionally, by tuning the lipid composition, mature fibril content decreased up to 74% and the ß-sheet content of Aß was significantly reduced. The reduction in fibril and ß-sheet content was consistent with a decrease in fibril diameter and could be attributed to the chaperone-like activity of the mixed vesicles. While demonstrating this remarkable activity, our findings present new evidence that lipid composition has a significant effect on the strength of the interaction between lipid bilayers and Aß peptides/fibrils. This understanding has intriguing therapeutic implications in treating protein misfolding diseases.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfolipídeos / Agregados Proteicos / Amiloide Tipo de estudo: Prognostic_studies Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfolipídeos / Agregados Proteicos / Amiloide Tipo de estudo: Prognostic_studies Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos