SKIPPERAD
"Simulation of the Kinetics and Inverse Problem for the Protein PolymERization in Amyloid Diseases (Prion, Alzheimer’s)"
| Coordinatore | INSTITUT NATIONAL DE RECHERCHE EN INFORMATIQUE ET EN AUTOMATIQUE
Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie. |
| Nazionalità Coordinatore | France [FR] |
| Totale costo | 1˙203˙569 € |
| EC contributo | 1˙203˙569 € |
| Programma | FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | ERC-2012-StG_20111012 |
| Funding Scheme | ERC-SG |
| Anno di inizio | 2012 |
| Periodo (anno-mese-giorno) | 2012-12-01 - 2017-11-30 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
INSTITUT NATIONAL DE LA RECHERCHE AGRONOMIQUE
Organization address
address: Rue De L'Universite 147 contact info |
FR (PARIS CEDEX 07) | beneficiary | 171˙000.00 |
| 2 |
INSTITUT NATIONAL DE RECHERCHE EN INFORMATIQUE ET EN AUTOMATIQUE
Organization address
address: Domaine de Voluceau, Rocquencourt contact info |
FR (LE CHESNAY Cedex) | hostInstitution | 1˙032˙569.00 |
| 3 |
INSTITUT NATIONAL DE RECHERCHE EN INFORMATIQUE ET EN AUTOMATIQUE
Organization address
address: Domaine de Voluceau, Rocquencourt contact info |
FR (LE CHESNAY Cedex) | hostInstitution | 1˙032˙569.00 |
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Obiettivo del progetto (Objective)
'Amyloid diseases are of increasing concern in our aging society. These diseases all involve the aggregation of misfolded proteins, called amyloid, which are specific for each disease (PrP for Prion, Abeta for Alzheimer's). When misfolded these proteins propagate the abnormal configuration and aggregate to others, forming very long polymers also called fibrils. Elucidating the intrinsic mechanisms of these chain reactions is a major challenge of molecular biology: do polymers break or coalesce? Do specific sizes polymerize faster? What is the size of the so-called nucleus, i.e., the minimum stable size for polymers? On which part of the reactions should a treatment focus to arrest the disease ? Up to now, only very partial and partially justified answers have been provided. This is mainly due to the extremely high complexity of the considered processes, which may possibly involve an infinite number of species and reactions (and thus, an infinite system of equations).
The great challenge of this project is to design new mathematical methods in order to model fibril reactions, analyse experimental data, help the biologists to discover the key mechanisms of polymerization in these diseases, predict the effects of new therapies. Our approach is based on a new mathematical model which consists in the nonlinear coupling of a size-structured Partial Differential Equation (PDE) of fragmentation-coalescence type, with a small number of Ordinary Differential Equations. On the one hand, we shall solve new and broad mathematical issues, in the fields of PDE analysis, numerical analysis and statistics. These problems are mathematically challenging and have a wide field of applications. On the other hand we want to test their efficacy on real data, thanks to an already well-established collaboration with a team of biophysicists. With such a continuing comparison with experiments, we aim at constantly aligning our mathematical problems to biological concerns.'