MECHCOMM

Mechanotransduction in Cell-to-Cell Communication

 Coordinatore KAROLINSKA INSTITUTET 

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

 Nazionalità Coordinatore Sweden [SE]
 Totale costo 2˙292˙100 €
 EC contributo 2˙292˙100 €
 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-2013-CoG
 Funding Scheme ERC-CG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-06-01   -   2019-05-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    KAROLINSKA INSTITUTET

 Organization address address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177

contact info
Titolo: Dr.
Nome: Ana Isabel
Cognome: De Sousa Teixeira
Email: send email
Telefono: 46852487979
Fax: +46 833 93 80

SE (STOCKHOLM) hostInstitution 2˙292˙100.00
2    KAROLINSKA INSTITUTET

 Organization address address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177

contact info
Titolo: Ms.
Nome: Riitta
Cognome: Ljungström
Email: send email
Telefono: +46 8 524 873 21

SE (STOCKHOLM) hostInstitution 2˙292˙100.00

Mappa


 Word cloud

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

outcomes    tumour    mechanical    roles    dna    pathway    diversity    ephrin    ligand    receptor    signalling    communication    inputs    eph    spatial    nanoclusters    origami    cells    pathways    cellular    organization    cell    mechanisms    generate    physical   

 Obiettivo del progetto (Objective)

'Cell-to-cell communication pathways coordinate cellular functions in multicellular organisms. Cells that are nearest neighbours can communicate through specific interactions between ligand and receptor proteins present in their respective cell membranes. The objective of this research program is to address the hypothesis that the physical context of the ligand/receptor interaction contributes to defining the fundamental mechanisms of action of cell-to-cell communication pathways and their cellular outcomes. The research program relies on the development of tools that provide well-defined physical inputs to cells, not confounded by simultaneous changes in chemical inputs. Therefore, beyond state-of-the-art developments in nanotechnology are here integrated with cell biology. In particular, DNA origami technology is applied to the development of ligand nanoclusters with customized spatial organization and mechanical properties. These ligand nanoclusters are used to probe the roles of physical properties of the ligand presentation on the activation of intracellular signalling pathways. We will focus on the ephrin/Eph cell-to-cell communication pathway, which regulates embryonic development and the homeostasis of adult organs. ephrin/Eph signalling is commonly disrupted in cancer, showing tumour suppressing or tumour promoting character. The mechanisms that generate the diversity of outcomes of the ephrin/Eph pathway are largely unknown. We will use DNA origami/ephrin ligand nanoclusters to investigate whether the spatial organization and mechanical properties of ephrin ligand assemblies impact Eph receptor function and contribute to generating diversity in the pathway. Our novel approach is readily transferrable to the study of other signalling pathways. We aim to generate a knowledge foundation for the roles of mechanotransduction, the conversion of physical to biochemical signals, in cell-to-cell communication mediated by membrane-bound ligands and receptors.'

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

CCC (2012)

Cracking the Cerebellar Code

Read More  

GLYCOTRACKER (2013)

"Tracking Glycosylations with Targeted, Molecule-Sized “Noses”"

Read More  

EURECIA (2009)

Understanding and Assessing the Impact and Outcomes of the ERC Funding Schemes

Read More