HOLOSTED

Combining holographic optogenetics and STED microscopy for studying synaptic plasticity in Alzheimer ’s disease

 Coordinatore CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE 

 Organization address address: Rue Michel -Ange 3
city: PARIS
postcode: 75794

contact info
Titolo: Mr.
Nome: Franck
Cognome: Charron
Email: send email
Telefono: +33 1 49 60 49 35
Fax: +33 1 49 60 41 46

 Nazionalità Coordinatore France [FR]
 Totale costo 193˙594 €
 EC contributo 193˙594 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2011-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-03-01   -   2014-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE

 Organization address address: Rue Michel -Ange 3
city: PARIS
postcode: 75794

contact info
Titolo: Mr.
Nome: Franck
Cognome: Charron
Email: send email
Telefono: +33 1 49 60 49 35
Fax: +33 1 49 60 41 46

FR (PARIS) coordinator 193˙594.80

Mappa


 Word cloud

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

era    stimulation    optical    plasticity    fellow    imaging    holography    synaptic    digital    sted    microscopy    super    first    optogenetics    holosted    germany    resolution    training    ad    wavefront    neuronal   

 Obiettivo del progetto (Objective)

'New perspectives are opening in neuroscience: the era of electricity is transitioning into the era of light. Super-resolution microscopy was elected “Method of the year 2008” and optogenetics “Method of the year 2010” by the Journal Nature Methods.

HOLOSTED is a biophysics project using these modern optical methods to study the effects of Alzheimer’s disease (AD) on synaptic plasticity. It has two general objectives: First, improving optical methods, including STED (STimulated Emission Depletion) microscopy and wavefront shaping. For the first time, digital holography will be combined with STED microscopy. This will enable precise control of synaptic signaling and the simultaneous analysis of the neuronal response with high spatial and temporal resolution. Second, progressing the understanding of AD by examining - on the level of single dendritic spines - the role of Amyloid beta, a central protein in AD, in compromising synaptic plasticity. The potential of certain drugs to rescue plasticity will be tested.

HOLOSTED provides training through research: The host, a leading lab in wavefront engineering for neuronal stimulation, will teach the fellow digital holography for optical stimulation of neurons by optogenetics or neurotransmitter uncaging. The fellow will not only be trained in physical methods, but also in biological application. Besides optics, he will learn neurophysiology and -pathology. Together with his background in super-resolution imaging this training will enable him to create a profile in Functional Super-Resolution Imaging for becoming an independent group leader.

HOLOSTED creates genuine mobility and thereby enables the fellow to transfer expertise of super-resolution microscopy to France and, upon his return, competence about targeted stimulation and optogenetics to Germany. Favored by contacts from previous stays in different countries (Greece, USA, Germany) the fellow will tighten scientific and personal relationships between peoples.'

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