http://www.cnr.it/ontology/cnr/individuo/prodotto/ID298998
Resveratrol interferes with the aggregation of membrane-bound human-IAPP: A molecular dynamics study (Articolo in rivista)
- Type
- Label
- Resveratrol interferes with the aggregation of membrane-bound human-IAPP: A molecular dynamics study (Articolo in rivista) (literal)
- Anno
- 2015-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.ejmech.2015.01.047 (literal)
- Alternative label
Fabio Lolicato a, b, Antonio Raudino a, Danilo Milardi c, *, Carmelo La Rosa a, * (2015)
Resveratrol interferes with the aggregation of membrane-bound human-IAPP: A molecular dynamics study
in European journal of medicinal chemistry (Online)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Fabio Lolicato a, b, Antonio Raudino a, Danilo Milardi c, *, Carmelo La Rosa a, * (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- a Department of Chemical Sciences, University of Catania, Viale A. Doria 6, Catania I-95125, Italy
b Department of Physics, Tampere University of Technology, P.O. Box 692, FI-33101 Tampere, Finland
c Istituto di Biostrutture e Bioimmagini, CNR, Unità Organizzativa e di Supporto di Catania, Viale A. Doria 6, Catania I-95125, Italy (literal)
- Titolo
- Resveratrol interferes with the aggregation of membrane-bound human-IAPP: A molecular dynamics study (literal)
- Abstract
- Amyloid aggregation of islet amyloid polypeptide (IAPP) in pancreatic tissues is a typical feature of type 2
diabetes mellitus. Resveratrol, a natural product extensively studied for its wide range of biological effects,
has been shown to inhibit IAPP aggregation. However, the mechanism by which resveratrol inhibits
IAPP aggregation is still far from complete elucidation. Now, an increasing knowledge of the mechanism
of amyloid toxicity shifts the target of research towards the development of compounds which can
prevent amyloid-mediated membrane damage rather than merely inhibit fiber formation. In this study
we used all atom molecular dynamics to investigate the interaction of resveratrol with full-length human
IAPP in a negatively charged membrane environment. Our results show that the presence of resveratrol
induces the formation of secondary structures (sheets and helices) by inserting in a hydrophobic pocket
between the interaction surface of two IAPP molecules in aqueous solution. On the other hand,
resveratrol significantly perturbs the interaction of IAPP with negatively charged membranes by
anchoring specific hydrophobic regions (23FGA25 and 32VGS34) of the peptide and forming a stable 1:2
IAPP:resveratrol complex at the water/membrane interphase. (literal)
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