FAR-QUAD

FoldAmeRs : a new family of G-QUADruplex ligands

 Coordinatore UNIVERSITE BORDEAUX I 

 Organization address address: 351 Cours de la Liberation
city: TALENCE
postcode: 33405

contact info
Titolo: Ms.
Nome: Patricia
Cognome: Dulor
Email: send email
Telefono: +33 (0)5 40 00 61 61
Fax: +33 (0)5 40 00 22 00

 Nazionalità Coordinatore France [FR]
 Totale costo 0 €
 EC contributo 174˙535 €
 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) 2009-03-01   -   2011-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE BORDEAUX I

 Organization address address: 351 Cours de la Liberation
city: TALENCE
postcode: 33405

contact info
Titolo: Ms.
Nome: Patricia
Cognome: Dulor
Email: send email
Telefono: +33 (0)5 40 00 61 61
Fax: +33 (0)5 40 00 22 00

FR (TALENCE) coordinator 174˙535.75

Mappa


 Word cloud

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

telomeric    cancer    quadruplex    ligands    telomerase    promising    groups    chemistry    structure    compound    human    quadruplexes    strategy    dna    anti   

 Obiettivo del progetto (Objective)

'This proposal focuses on the formation of complex between DNA G-quadruplexes and a new family of synthetic ligands, which might be relevant for cancer therapy. The enzymatic acitivity of telomerase is critical to the immortality of most human cancer cell lines. However, telomeric DNA may fold into guanine quadruplex structures which are not competent substrates for telomerase. Therefore, the use of small molecule ligands to induce quadruplex stabilisation in telomeric DNA has potential as an anti-cancer strategy. A European collaboration recently engaged between I. Huc (Bordeaux, France) and S. Balasubramanian (Cambridge, UK) groups already led to the identification of a very promising compound, with exceptionnal potential for stabilising human G-quadruplex telomer. In addition a three dimensionnal helical compound (foldamer) has shown interesting activity. This project, involving chemistry, biology and biophysic, aims i) to systematically design and develop new analogues of this promising candidate, based on aromatic delta-peptide chemistry; ii) to evaluate their G-quadruplex binding affinity in telomere and others systems; iii) to establish structure-activity relationships; iv) to determine the key elements necessary for specific G-quadruplex recognition by solving the structure of the first ligand complexed with G-quadruplex. This original interdisciplinary proposal involves two international leading groups in their respective field, to develop new tools and knowledge on the growing interest on natural G-quadruplexes as new target for anti-cancer strategy. The applicant will have a crucial role in the development of this collaboration and will become an active and efficient third partner, when returning back to China at the end of the fellowship.'

Introduzione (Teaser)

Telomeres are repetitive sequences of DNA at the end of chromosomes that protect our genetic information from certain harmful interactions. In this way, they have been likened to the plastic tips on shoelaces.

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