SUPRACHEMBIO

Supramolecular Chemical Biology Modulation of Protein-Protein Interactions

 Coordinatore  

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Non specificata
 Totale costo 1 €
 EC contributo 0 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-07-01   -   2013-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITEIT EINDHOVEN

 Organization address address: DEN DOLECH 2
city: EINDHOVEN
postcode: 5612 AZ

contact info
Titolo: Dr.
Nome: Lucas
Cognome: Brunsveld
Email: send email
Telefono: +49 231 97426473
Fax: +49 231 1332499

NL (EINDHOVEN) hostInstitution 0.00
2    TECHNISCHE UNIVERSITEIT EINDHOVEN

 Organization address address: DEN DOLECH 2
city: EINDHOVEN
postcode: 5612 AZ

contact info
Titolo: Mr.
Nome: Rob
Cognome: Debey
Email: send email
Telefono: +31 40 2473787
Fax: +31 40 2472206

NL (EINDHOVEN) hostInstitution 0.00

Mappa


 Word cloud

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

interactions    protein    cells    chemistry    platform    architectures    outlined    multivalent    combination    proteins    assembling    introduction    chemical    cellular    scaffolds    localization    modulation    self    biology    supramolecular   

 Obiettivo del progetto (Objective)

'This proposal aims to explore the combination of supramolecular chemistry with chemical biology. Supramolecular architectures are proposed for the modulation of protein-protein interactions. Two general themes are outlined; 1) supramolecular chemistry in the cell and 2) supramolecular multivalency. Supramolecular architectures are brought forward as excellent tools to control protein-protein interactions at the cellular level. Supramolecular elements, selectively attached to proteins, are outlined to control protein dimerization and localization. The introduction of different supramolecular elements, either in vitro or in vivo via specific labeling techniques, is part of the plan, including the introduction of supramolecular elements, whose interactions can be reversibly switched with light. With these systems, the temporal control over protein-protein interactions and protein localization can be addressed. Self-assembling multivalent architectures are proposed as optimal scaffolds and flexible systems for recognition and binding of cells. The assembly process of the supramolecular architecture will be steered via interplay with the characteristics of the cellular target and the environment, controlling size, shape and composition. This self-assembling multivalent platform will be applied to control or initiate interactions between different types of surfaces, such as cells, antigens and chips. The self-assembling scaffolds additionally provide an ideal platform to be combined with proteins, allowing the generation of ordered protein wires, with control over orientation and distances between proteins. The combination of supramolecular chemistry with chemical biology is envisioned to enable the modulation of protein-protein interactions and thus provide entries to this long standing fundamental challenge.'

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