Amyloid fibrils are highly ordered aggregates whose formation occurs during the development of several serious disorders, like Althzeimer's and Parkinson's diseases. Even if most biophysical investigations of fibril formation have attempted to elucidate the structural events that occur during amyloid fibril assembly, relatively little is known about the thermodynamics of the aggregated protein state, and the kinetic mechanisms of its formation. Fibrillation is an irreversible process and a key challenge for the field is the development of therapeutic strategies able to inhibit or reverse the aggregation. The coupling of conventional Fourier Transform Infrared Spectroscopy (FTIR) and high Pressure (HP) techniques has proven to be during the last years a perfect combination for the study of proteins aggregation and misfolding, allowing to explore proteins conformational states not accessible at ambient pressure. In contrast to temperature, whose effect manifests both on volume and thermal energy simultaneously, pressure leads to a controlled change of inter- and intramolecular distances and enables to determine the stability of a protein structure and to stabilize intermediate states that are usually not detectable at ambient pressure or through thermal perturbation. Due to its effect on the energetic of the system, a pressure increase will act on packing defects and empty cavities favouring all that processes that lead to a reduction of the system's volume. We present here the HP-induced disaggregation of two amyloidogenic proteins, insulin and a-synuclein. Insulin aggregation into amyloid-like structures represents a serious problem in its storage as pharmaceutical for the treatment of diabetes mellitus while the interest in studying a- synuclein resides in its involvement in Parkinson's disease. According to our experimental evidences high pressure induces the disaggregation of fibrils with an efficacy that depends on their maturation stage in the case of insulin and on the specific point mutation occurred in protein primary structure in the case of synuclein. Moreover, high pressure dissociation has been found to act in a sequential way, in accordance with the hierarchy of structures.
|Titolo:||FTIR studies of the high pressure dissociation of insulin and alpha-synuclein amyloids|
|Autori:||Piccirilli, F; Mangialardo, S; Perucchi, A; Lupi, S; Postorino, P; Plotegher, N; Ortore, M, G; Spinozzi, F; Mariani, P; Bubacco, L; Postorino, P; Lupi, S; Perucchi A|
|Data di pubblicazione:||2012|
|Settore Scientifico Disciplinare:||Settore FIS/07 - Fisica Applicata(Beni Culturali, Ambientali, Biol.e Medicin)|
|Citazione:||Piccirilli, F., Mangialardo, S., Perucchi, A., Lupi, S., Postorino, P., Plotegher, N., et al. (2012). FTIR studies of the high pressure dissociation of insulin and alpha-synuclein amyloids [Altro].|
|Tipologia di ateneo:||10 - Abstract di Comunicazioni o Poster di Congressi nazionali pubblicati (anche on line)|
|Appare nelle tipologie:||99 - Altro|