ANTI-VIROME

"A combined evolutionary and proteomics approach to the discovery, induction and application of antiviral immunity factors"

 Coordinatore UNIVERSITAET ULM 

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

 Nazionalità Coordinatore Germany [DE]
 Totale costo 1˙915˙200 €
 EC contributo 1˙915˙200 €
 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-2012-ADG_20120314
 Funding Scheme ERC-AG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-04-01   -   2018-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET ULM

 Organization address address: HELMHOLTZSTRASSE 16
city: ULM
postcode: 89081

contact info
Titolo: Mr.
Nome: Frank
Cognome: Gleixner
Email: send email
Telefono: +49 731 500 66397
Fax: +49 731 500 66392

DE (ULM) hostInstitution 1˙915˙200.00
2    UNIVERSITAET ULM

 Organization address address: HELMHOLTZSTRASSE 16
city: ULM
postcode: 89081

contact info
Titolo: Prof.
Nome: Frank
Cognome: Kirchhoff
Email: send email
Telefono: +49 731 500 65150
Fax: +49 731 500 65153

DE (ULM) hostInstitution 1˙915˙200.00

Mappa


 Word cloud

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

human    evolved    hiv    immunity    capability    aids    positive    effectors    pathogens    pandemic    inducers    antiviral    pressure    evolutionary    therapeutic    counteract    invading    restriction    induction    intrinsic   

 Obiettivo del progetto (Objective)

'Humans are equipped with a variety of intrinsic immunity or host restriction factors. These evolved under positive selection pressure for diversification and represent a first line of defence against invading viruses. Unfortunately, however, many pathogens have evolved effective antagonists against our defences. For example, the capability of HIV-1 to counteract human restriction factors that interfere with reverse transcription, uncoating and virion release has been a prerequisite for the global spread of AIDS. We are just beginning to understand the diversity and induction of antiretroviral factors and how pandemic HIV-1 group M (major) strains evolved to counteract all of them. Here, I propose to use a genetics, proteomics and evolutionary approach to discover and define as-yet-unknown antiviral effectors and their inducers. To identify novel antiviral factors, we will examine the capability of all primate genes that are under strong positive selection pressure to inhibit HIV and its simian (SIV) precursors. This examination from the evolutionary perspective of the invading pathogen will also reveal which adaptations allowed HIV-1 to cause the AIDS pandemic. Furthermore, complex peptide-protein libraries representing essentially the entire human peptidome, will be utilized to identify novel specific inducers of antiviral restriction factors. My ultimate aim is to unravel the network of inducers and effectors of antiviral immunity - the 'Anti-Virome' - and to use this knowledge to develop novel effective preventive and therapeutic approaches based on the induction of combinations of antiviral factors targeting different steps of the viral life cycle. The results of this innovative and interdisciplinary program will provide fundamental new insights into intrinsic immunity and may offer alternatives to conventional vaccine and therapeutic approaches because most restriction factors have broad antiviral activity and are thus effective against various pathogens.'

Altri progetti dello stesso programma (FP7-IDEAS-ERC)

ORDER IN DISORDER (2012)

Order in Disorder: Context-dependent strategies for integrating peptide-mediated interactions

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VSSC (2013)

Verifying and Synthesizing Software Compositions

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NANO@ENERGY (2011)

Novel Design of Nanostructures for Renewable Energy: Fundamental Questions and Advanced Applications

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