UB-DECODED

Deciphering the ubiquitin code of the TNF receptor signalling complex and its functional role in inflammation and immunity

 Coordinatore UNIVERSITY COLLEGE LONDON 

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 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 2˙367˙337 €
 EC contributo 2˙367˙337 €
 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)
 Code Call ERC-2011-ADG_20110310
 Funding Scheme ERC-AG
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-04-01   -   2017-03-31

 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: Tatjana
Cognome: Palalic
Email: send email
Telefono: +44 20 7594 3866

UK (LONDON) beneficiary 627˙725.10
2    UNIVERSITY COLLEGE LONDON

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Ms.
Nome: Malgorzata
Cognome: Kielbasa
Email: send email
Telefono: 442031000000
Fax: 442078000000

UK (LONDON) hostInstitution 1˙739˙611.90
3    UNIVERSITY COLLEGE LONDON

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Prof.
Nome: Henning
Cognome: Walczak
Email: send email
Telefono: +44 207 679 6471
Fax: +44 207 679 6425

UK (LONDON) hostInstitution 1˙739˙611.90

Mappa


 Word cloud

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code    linkages    molecularly    immunity    infection    inflammation    pathological    rsc    signalling    physiological    cancer    decipher    chain    linkage    tnf    functions    ubiquitin   

 Obiettivo del progetto (Objective)

'Tumour necrosis factor (TNF) is a cytokine with important functions in inflammation, immunity and cancer. Signalling processes mediated by ubiquitin are crucial for TNF signalling. The seven lysine (K) residues and the N-terminus of ubiquitin can be used to form ubiquitin chains. Employing a method newly developed in our laboratory we identified the presence of four of these ubiquitin chain linkage types in the native TNF receptor signalling complex (TNF-RSC). Our knowledge of the specific functions of the different ubiquitin linkages is currently very limited. However, their presence in the TNF-RSC, combined with our recent technological advance in dissecting the composition of this protein complex with previously unreached specificity and sensitivity provides a unique opportunity for the proposed research programme: to molecularly and functionally decipher the ubiquitin code. We will aim to achieve this by studying the different ubiquitin chain linkages at the molecular level within the TNF-RSC and by determining how perturbation of specific ubiquitin linkage events impacts the physiological role of TNF in immunity to infection and its pathological function in inflammation-induced cancer. The specific objectives of this project are: • to molecularly decipher the ubiquitin code of the TNF-RSC (objective 1), • to link this code to physiological functions of TNF in immunity to infection (objective 2) • and to test its pathological impact on cancer-related inflammation (objective 3).'

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