Objective
The objective of this proposal is to coordinate the establishment of a European resource infrastructure of binding molecules directed against the entire human proteome. A major objective of the post-genome era is to detect, quantify and characterise all relevant human proteins in tissues and fluids in health and disease. This effort requires a comprehensive, characterised and standardised collection of specific ligand-binding reagents, including antibodies; the most widely used such molecules, as well as novel protein scaffolds and nucleic acid aptamers.
Currently there is no pan-European platform to coordinate systematic development, resource management and quality control for these important reagents. This CA will coordinate 25 European partners and two in the USA, several of which operate infrastructures or large-scale projects in aspects including cDNA collections, protein production, polyclonal and monoclonal antibodies. They provide a critical mass of leading expertise in binder technology, protein expression, binder applications and bioinformatics. Many have tight links to relevant SMEs, as founders or advisors.
The CA will plan the organisation of the resource, by integrating existing infrastructures, reviewing technologies and high throughput production methods, standardising binder-based tools and applications, assembling bioinformatics and establishing a database schema for a central binders repository. The proteome binders' resource is predicted to have huge benefits for basic and applied research, impacting on healthcare, diagnostics, target discovery for drug intervention and therapeutics.
It will thus be of great advantage to the research and biotechnology communities. In general terms, Europe is already well advanced in the technologies required and excellently placed to initiate this large-scale project. The CA will prepare the way for an application for the production phase of the infrastructure under FP7.
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.
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.
- natural sciences biological sciences biochemistry biomolecules proteins proteomics
- natural sciences biological sciences biochemistry biomolecules nucleic acids
- natural sciences computer and information sciences databases
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Programme(s)
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
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.
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.
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
FP6-2004-INFRASTRUCTURES-5
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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.
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.
IA-CA - Integrating activities implemented as Coordination Actions
Coordinator
CAMBRIDGE
United Kingdom
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Participants (29)
PARIS
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GLASGOW
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HEIDELBERG
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HEIDELBERG
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BRAUNSCHWEIG
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KASSEL
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KONSTANZ
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STOCKHOLM
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PO Box 9600 LEIDEN
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LOS ALAMOS, NEW MEXICO
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117 LUND
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MUENCHEN
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REUTLINGEN
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RIJEKA
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DUBLIN
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BERLIN
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BOULDER, CO
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BRAUNSCHWEIG
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MUENCHEN
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UPPSALA
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ZWIJNAARDE
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1000 ESPOO
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LONDON
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ZURICH
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CAMBRIDGE
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BERLIN
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TALENCE
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NEUHERBERG
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BORDEAUX
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