PEPTIDE OSTEOGEL

Determining novel peptide sequence and matrix mechanical properties to increase osteogenesis in embryonic stem cells using designer alginate hydrogels for bone regeneration

 Coordinatore IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE 

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Mr.
Nome: Shaun
Cognome: Power
Email: send email
Telefono: +44 20 7594 8773
Fax: +44 20 7594 8609

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 201˙049 €
 EC contributo 201˙049 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2010-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-03-01   -   2013-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Mr.
Nome: Shaun
Cognome: Power
Email: send email
Telefono: +44 20 7594 8773
Fax: +44 20 7594 8609

UK (LONDON) coordinator 201˙049.60

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

cell    hydrogel    peptide    proteins    dimensional    alginate    bone    osteogenesis    sequences    osteogenic    stiffness    induce    escs    osteoblasts    stem    differentiation    mechanical    then    matrix    medicine    regenerative    maximize   

 Obiettivo del progetto (Objective)

'Regenerating large bone defects is a great challenge in regenerative medicine. Embryonic stem cell (ESC) therapies are an attractive option due to their unlimited proliferation and ability to produce the cell types needed for bone repair. Here, we propose creating a three-dimensional alginate hydrogel that displays bioactive epitopes and has mechanical properties that induce osteogenic differentiation of ESCs and increase bone formation in vitro. We will do this by building upon previous research in the group of Prof Molly Stevens, which found that ESCs cultured on the extracellular matrix of bone forming osteoblasts increased both differentiation into osteogenic cells and bone formation. We propose using a proteomic approach to identify the proteins that are responsible for this effect. Once the proteins are known, they will be cut into short overlapping peptides that will be synthesized and attached to a cell culture surface. ESCs will then be grown on them to determine the sequences that induce osteogenesis. Using two-dimensional hydrogels of different stiffness that are coated with the osteogenic peptide, the mechanical properties that maximize osteogenesis will be determined. This peptide will then be coupled to alginate to form a hydrogel whose mechanical properties will be tailored to maximize bone formation. Novel sequences which induce osteogenesis are important to stem cell biology and an artificial matrix that differentiates ESCs into osteoblasts using both displayed ligands and stiffness would be important to regenerative medicine. The project Peptide Osteogel will be beneficial to Europe by bringing a scientist with a unique skill set into a top biomaterials lab to work on a multidisciplinary project that will increase the quality and status of science in the European Union. This fellowship will enable greater collaboration and transfer of knowledge across Europe, increasing the mobility and human potential of scientists across the continent.'

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