SBPSSHS

Structural Basis of Protein Synthesis System of Human Cell

 Coordinatore CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE 

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 Nazionalità Coordinatore France [FR]
 Totale costo 2˙466˙000 €
 EC contributo 2˙466˙000 €
 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    CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE

 Organization address address: Rue Laurent Fries 1
city: ILLKIRCH GRAFFENSTADEN
postcode: 67404

contact info
Titolo: Dr.
Nome: Marat
Cognome: Yusupov
Email: send email
Telefono: +33 3 88 65 33 01
Fax: +33 3 88 65 32 78

FR (ILLKIRCH GRAFFENSTADEN) hostInstitution 2˙466˙000.00
2    CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE

 Organization address address: Rue Laurent Fries 1
city: ILLKIRCH GRAFFENSTADEN
postcode: 67404

contact info
Titolo: Dr.
Nome: Steve
Cognome: Brooks
Email: send email
Telefono: +33 3 88 65 33 94
Fax: +33 3 88 65 32 03

FR (ILLKIRCH GRAFFENSTADEN) hostInstitution 2˙466˙000.00

Mappa


 Word cloud

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

determination    structures    ratcheted    human    structural    resolution    first    investigation    eukaryotic    ray    complexes    ribosome    mechanism       yeast    crystal    functional    crystals    determine    step    ribosomes    atomic    biochemical    mrna       obtain    cells    structure    trna    translocation    hela    initiation   

 Obiettivo del progetto (Objective)

'This project will elucidate the structure and mechanism of ribosome function through the determination of high resolution crystal structures of human ribosome functional complexes. Currently, the only high resolution crystal structures available for the ribosome functional complexes are bacterial ribosomes containing mRNA, tRNAs in E, P and A sites and several translation factors. Recently, we have determined at medium resolution the first eukaryotic ribosome structure. Saccharomyces cerevisaiae ribosomes have been chosen for the first step of the study because they have been extensively investigated in our laboratory by biochemical methods and by x-ray analysis. Step One: We will improve the quality of the crystals and determine the ribosome structure of yeast at atomic resolution (about 3Å resolution). These conditions will be used for an investigation of the ribosome functional complexes in order to better understand the detailed mechanism of the translocation of large molecules (tRNA and mRNA) on the ribosome. Step Two: Ribosomes from human HeLa cells will be investigated via crystallization and x-ray structure determination. Ribosome functional complexes developed on yeast systems will be used as models for the creation and structural investigation of human ribosome complexes. Available biochemical data will provide a framework for the interpretation of structural information which will be obtained. The aims: To determine the atomic resolution crystal structure of the yeast ribosome as a model for all eukaryotic ribosome x-ray studies. To obtain crystals and determine the structure of 80S ribosome from HeLa cells. To determine the structure of the ribosome complexes with mRNA and tRNA in ratcheted and non-ratcheted states in order to describe the mechanism of translocation. To determine structure of the ribosome initiation complex with an internal ribosomal entry site mRNA. To obtain crystals and to determine the structures of 40S initiation complexes.'

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LATTICE (2008)

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DESERTSTORMS (2010)

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