NAMIC

Nanowire Atomic Force Microscopy for Real Time Imaging of Nanoscale Biological Processes

 Coordinatore ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE 

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 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 1˙264˙640 €
 EC contributo 1˙264˙640 €
 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-StG_20111012
 Funding Scheme ERC-SG
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-12-01   -   2017-11-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE

 Organization address address: BATIMENT CE 3316 STATION 1
city: LAUSANNE
postcode: 1015

contact info
Titolo: Ms.
Nome: Caroline
Cognome: Vandevyver
Email: send email
Telefono: +41 21 693 4977
Fax: +41 21 693 55 85

CH (LAUSANNE) hostInstitution 1˙264˙640.40
2    ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE

 Organization address address: BATIMENT CE 3316 STATION 1
city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Georg Ernest
Cognome: Fantner
Email: send email
Telefono: +41 21 693 64 31
Fax: ++41 21 6936910

CH (LAUSANNE) hostInstitution 1˙264˙640.40

Mappa


 Word cloud

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

nanoscale    afm    cells    molecular    obtain    resolution    cantilevers    science    life    tools    structures    speed    nanowire    living   

 Obiettivo del progetto (Objective)

'Short summary:

The ability to measure structures with nanoscale resolution continues to transform physics, materials science and life science alike. Nevertheless, while there are excellent tools to obtain detailed molecular-level static structure (for example in biology), there are very few tools to develop an understanding of how these structures change dynamically as they fulfill their biological function. New biologically-compatible, high-speed nanoscale characterization technologies are required to perform these measurements. In this project, we will develop a nanowire-based, high-speed atomic force microscope (NW-HS-AFM) capable of imaging the dynamics of molecular processes on living cells. We will use this instrument to study the dynamic pore-formation mechanisms of novel peptide antibiotics. This increase in performance over current AFMs will be achieved through the use of electron-beam-deposited nanogranular tunneling resistors on prefabricated nanowire AFM cantilevers. By combining these cantilevers with our state of the art high-speed AFM technology, we expect to obtain nanoscale-resolution images of protein pores on living cells at rates of tens of milliseconds per image. This capability will open a whole new arena for seeing nanoscale life in action.'

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