MICROBE

"Robustness, evolutionary optimality and plasticity of microbial signaling"

 Coordinatore  

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

 Nazionalità Coordinatore Non specificata
 Totale costo 2˙490˙000 €
 EC contributo 2˙490˙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 E
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-12-01   -   2016-11-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG

 Organization address address: SEMINARSTRASSE 2
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Mr.
Nome: Jürgen
Cognome: Auer
Email: send email
Telefono: +49 6221 546801
Fax: +49 6221 54 6809

DE (HEIDELBERG) beneficiary 917˙780.00
2    MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.

 Organization address address: Hofgartenstrasse 8
city: MUENCHEN
postcode: 80539

contact info
Titolo: Mr.
Nome: Christian
Cognome: Bengelsdorff
Email: send email
Telefono: +49 6421 178901
Fax: +49 6421 178909

DE (MUENCHEN) hostInstitution 1˙572˙220.00
3    MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.

 Organization address address: Hofgartenstrasse 8
city: MUENCHEN
postcode: 80539

contact info
Titolo: Prof.
Nome: Viktor
Cognome: Sourjik
Email: send email
Telefono: +49 152 09340856
Fax: +49 6421 178909

DE (MUENCHEN) hostInstitution 1˙572˙220.00

Mappa


 Word cloud

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biological    function    signaling    cellular    robustness    levels    perturbations    functions    network    networks    quantitative    plasticity    protein    performance    evolutionary   

 Obiettivo del progetto (Objective)

'Most signaling and regulatory functions in the cell are executed by protein networks rather than by individual proteins, and it is therefore essential for biology to understand how the design and function of these networks have been shaped by the evolution. Despite differences in biological functions and molecular composition, all protein networks underlie similar evolutionary constrains on their performance and design, such as necessity to be robust against extra- and intracellular perturbations or to extract information from noisy environment. Moreover, although it can be assumed that a particular network has evolved to optimally solve certain problem, detailed quantitative analyses of optimality of the network performance are largely missing. Similarly little explored is the question of the network plasticity: how networks adapt to changing environmental conditions by adjustments of their structure and function, either regulating protein levels or undergoing microevolutionary changes. The goal of this proposal is to elucidate general features responsible for robustness and plasticity of cellular networks, using signaling networks in bacteria and yeast as well-tractable and relatively simple model systems. To achieve that, we will combine quantitative real-time analyses of the network function, primarily using high-throughput fluorescence microscopy, with computational modeling and with experimental microevolution, while exposing the networks to such common intra- and extracellular perturbations as variations in protein levels and in temperature. We expect our comparative analysis to provide general insights into the mechanisms of robustness and evolutionary optimization of cellular networks, thereby substantially advancing our understanding of biological systems.'

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