Articolo in rivista, 2008, ENG, 10.1016/j.abb.2008.06.018
Michele Francesco Maria Sciacca;a Matteo Pappalardo;a Danilo Milardi;b Domenico M. Grasso;a Carmelo La Rosa;a*
a Dipartimento di Scienze Chimiche, Universita' di Catania, Viale Andrea Doria 6, 95125 Catania, Italy b Istituto CNR di Biostrutture e Bioimmagini--Sezione di Catania, Viale Andrea Doria 6, 95125 Catania, Italy
The role played by Ca2+ ions in the interaction of the human islet amyloid polypeptide (hIAPP) with model membranes has been investigated by differential scanning calorimetry (DSC) and circular dichroism (CD) experiments. In particular, the interaction of hIAPP and its rat isoform (rIAPP) with zwitterionic dipalmitoyl-phosphatidylcholine (DPPC), negatively charged dipalmitoyl-phosphatidylserine (DPPS) vesicles and with a 3:1 Mixtures of them, has been studied in the presence of Ca2+ ions. The experiments have evidenced that amorphous, Soluble NAPP assemblies interact with the hydrophobic core of DPPC bilayers. Conversely, the presence of Ca2+ ions is necessary to activate a preferential interaction of hIAPP with the hydrophobic core of DPPS membranes. These findings support the hypothesis that an impaired cellular homeostasis of Ca2+ ions may promote the insertion of NAPP into the hydrophobic core of carrier vesicles which is thought to contribute to an eventual intracellular accumulation of beta-sheet rich hIAPP aggregates.
Archives of biochemistry and biophysics (Print) 47 , pp. 291–298
differential scanning calorimetry, polypeptides, membranes, metal ions, thermotropic properties
ID: 13939
Year: 2008
Type: Articolo in rivista
Creation: 2009-07-16 00:00:00.000
Last update: 2012-05-02 09:07:55.000
CNR authors
CNR institutes
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:13939
DOI: 10.1016/j.abb.2008.06.018
ISI Web of Science (WOS): 000259170000015