Skip to main content
Go to the home page of the European Commission (opens in new window)
English English
CORDIS - EU research results
CORDIS
Content archived on 2024-06-18

Protein aggregation and toxicity in human diseases

Objective

This research project deals with the role of protein aggregation in several human diseases which are connected to the formation of fibrillar protein structures. Currently, no effective pharmaceutical treatment is available for these diseases, a fact which reflects our present lack of understanding of the molecular mechanism responsible for their formation and pathogenicity. This severe lack of knowledge is in large part a consequence of the lack of suitable tools to address these questions.
In this project, I propose a strategy to apply chemical kinetic analysis in combination with biophysics and biological assays to address the relationship between the mechanism of protein aggregation and its biological consequences. The study will focus on the amyloid-β peptide (Aβ), the peptide implicated in Alzheimer’s disease. The approach and the platform developed in this project will be also of relevance for a large number of other biological systems. I plan to build on the possibility open only recently by biophysical techniques to follow the time evolution of the concentration of the oligomers during the aggregation process and apply the chemical kinetic approach to measure the rate laws and identify the aggregation mechanism of the oligomers. In parallel, by performing kinetic experiments on toxicity I plan to apply the same strategy to identify the aggregation mechanism of the processes that generate toxicity, with the attractive prospective of improving our quantitative understanding of the mechanistic relationship between protein aggregation and its biological consequences. In a second stage of the project I plan to tackle the limitations of conventional biophysics in characterizing the oligomers by developing new biophysical tools based on microfluidic technology to allow the rapid characterization of heterogeneous samples in short time and improve the detection resolution of the oligomer population with respect to traditional approaches.

Fields of science (EuroSciVoc)

CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.

You need to log in or register to use this function

Topic(s)

Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.

Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

FP7-PEOPLE-2013-IEF
See other projects for this call

Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

MC-IEF - Intra-European Fellowships (IEF)

Coordinator

THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
EU contribution
€ 221 606,40
Address
TRINITY LANE THE OLD SCHOOLS
CB2 1TN CAMBRIDGE
United Kingdom

See on map

Region
East of England East Anglia Cambridgeshire CC
Activity type
Higher or Secondary Education Establishments
Links
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

No data
My booklet 0 0