ANTI-APOPTOTIC NLEH

"Investigating the anti-apoptotic properties of NleH, an effector of the diarrheagenic pathogens Enteropathogenic Escherichia coli (EPEC) and enterohaemorrhagic E. coli (EHEC)."

 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 182˙103 €
 EC contributo 182˙103 €
 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-2009-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-04-01   -   2012-03-31

 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 182˙103.20

Mappa


 Word cloud

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

effector    pathogens    escherichia    epec    ss    espf       apoptotic    ehec    protein    anti    nleh    coli   

 Obiettivo del progetto (Objective)

'Enteropathogenic Escherichia coli (EPEC) and enterohaemorrhagic Escherichia coli (EHEC) are closely related diarrheagenic pathogens that are important causes of morbidity and mortality worldwide, especially in young children. EPEC and EHEC are known as attaching and effacing pathogens because they intimately adhere to gut enterocytes and instigate effacement of brush border microvilli. Injection of bacterial effector proteins via a type III secretion system (T3SS) is an integral part of the EPEC and EHEC infection strategy. One such effector, EspF, binds and induces degradation of the anti-apoptotic protein AbcF2, however, although infected cells show early apoptotic symptoms, they do not present late apoptosis signs. The T3SS effectors NleH1 and NleH2 were recently found to have a broad range anti-apoptotic activity which may neutralise the effect of EspF and promote cell survival. In this proposal we wish to investigate the anti-apoptotic activity of NleH, in particular its binding to the endoplasmic reticulum (ER) anti-apoptotic protein Bax inhibitor-1 (BI-1) and to PDZ domain-containing protein/s.'

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