Coordinatore | Karlsruher Institut fuer Technologie
Organization address
address: Kaiserstrasse 12 contact info |
Nazionalità Coordinatore | Germany [DE] |
Totale costo | 5˙553˙931 € |
EC contributo | 3˙988˙730 € |
Programma | FP7-HEALTH
Specific Programme "Cooperation": Health |
Code Call | FP7-HEALTH-2011-two-stage |
Funding Scheme | CP-FP |
Anno di inizio | 2012 |
Periodo (anno-mese-giorno) | 2012-01-01 - 2014-12-31 |
# | ||||
---|---|---|---|---|
1 |
Karlsruher Institut fuer Technologie
Organization address
address: Kaiserstrasse 12 contact info |
DE (Karlsruhe) | coordinator | 609˙050.00 |
2 |
ISOGENICA LTD
Organization address
address: "The MANSION, CHESTERFORD RESEARCH PARK" contact info |
UK (LITTLE CHESTERFORD SAFFRON WALDEN) | participant | 700˙500.00 |
3 |
Center for Advanced Bioanalysis GmbH
Organization address
address: Scharitzerstrasse 6-8 contact info |
AT (Linz) | participant | 549˙000.00 |
4 |
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Organization address
address: University Offices, Wellington Square contact info |
UK (OXFORD) | participant | 499˙980.00 |
5 |
BIAMETRICS GMBH
Organization address
address: AUF DER MORGENSTELLE 18 contact info |
DE (TUBINGEN) | participant | 471˙000.00 |
6 |
PEPperPRINT GmbH
Organization address
address: Schlossweg 9 contact info |
DE (Wiesloch) | participant | 459˙000.00 |
7 |
APOGENIX GMBH
Organization address
address: IM NEUENHEIMER FELD 584 contact info |
DE (HEIDELBERG) | participant | 400˙000.00 |
8 |
DEUTSCHES KREBSFORSCHUNGSZENTRUM
Organization address
address: Im Neuenheimer Feld 280 contact info |
DE (HEIDELBERG) | participant | 130˙000.00 |
9 |
MICROSYSTEMS LTD
Organization address
address: kv. CHAIKA 15-D-21 contact info |
BG (Varna) | participant | 100˙000.00 |
10 |
TECHNICAL UNIVERSITY OF VARNA
Organization address
address: Studentska 1 contact info |
BG (VARNA) | participant | 70˙200.00 |
Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.
'We want to further develop our tools and technologies for high-throughput research, with the final goals being (I.) the particle-based combinatorial synthesis of 1 Mio different peptides on a glass slide for chemical costs of ~50€ (KIT, CBL, MS, TUV), and (II.) the labelling-free parallel readout of binding affinities by a variant reflectometric interference spectroscopy method for ~10.000 peptide spots per cm(2) when staining the array with an unlabeled protein (BIA, KIT). These tools provide the basis (III.) for a standardized, fast, and reliable high-throughput procedure that we want to develop in order to find high-affinity peptide binders against any pharmaceutically interesting target protein. Such a procedure might have an important impact in medicine and in the biotechnology industry. In order to achieve this goal, we will use display techniques that in combination with high-throughput sequencing typically will identify ~100.000 putative peptide binders per target protein (ISO). These will be synthesized in array format to validate binding to the target protein by an independent method (PPP, DKFZ). Next, based on binders from initial screens, many variant peptides are synthesized in high-density array format for iterative screens (PPP, DKFZ, KIT), whereby massive parallel labelling-free detection of binders pinpoints higher-affinity binders (BIA). In order to validate our novel high-throughput procedure, (IV.) we want to find high-affinity peptide binders against relevant target proteins (delivered by APO and OXF), and test these binders in biological assays (OXF, APO).'
High-throughput screening (HTS) can rapidly identify active compounds for specific targets in drug design, for example. EU research is developing ways to accelerate the process.
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