PHOSPHORECEPTORS

Synthesis of novel metallo-receptors for phosphorylated species via dynamic combinatorial chemistry

 Coordinatore IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE 

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

contact info
Titolo: Ms.
Nome: Brooke
Cognome: Alasya
Email: send email
Telefono: +44 20 7594 1181
Fax: +44 20 7594 1418

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 0 €
 EC contributo 172˙434 €
 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-IIF-2008
 Funding Scheme MC-IIF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-12-07   -   2011-12-06

 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: Ms.
Nome: Brooke
Cognome: Alasya
Email: send email
Telefono: +44 20 7594 1181
Fax: +44 20 7594 1418

UK (LONDON) coordinator 172˙434.64

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species    sensitivity    dynamic    combinatorial    cell    binding    receptors    interactions    combine    selectivity    phosphorylated    chemical    detection   

 Obiettivo del progetto (Objective)

'Phosphorylation of proteins and metabolites is an essential mechanism for signal transduction and propagation in the cell and thus of utmost importance for cellular function. In spite of this, there is a lack of synthetic chemical receptors for the detection and separation of phosphoesters that combine selectivity and sensitivity. In this project we aim to develop novel chemical receptors for the efficient recognition of phosphorylated molecules of biological interest. The design of such receptors will be based on metallo-receptors that combine strong binding (through metal-phosphate interactions) with high selectivity (provided by hydrogen-bonding groups and other reversible interactions). In order to assemble the different components of the receptors, we propose to use dynamic combinatorial chemistry (DCC) using the phosphorylated species of interest as templates to “amplify” the best receptors from the virtual dynamic combinatorial library. Once the best receptors are identified using the above methodology and their selectivity and sensitivity are optimised, they will be used for the development of chemical sensors to detect specific phosphorylated species. This will be carried out by incorporating optical labels that change their properties upon binding between receptor and phosphorylated guest. Particular emphasis will be given to the detection of phosphorylated phosphoinositides since they play important roles in cell signalling and regulation and their levels can be correlated to the molecular basis of certain diseases.'

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