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VCSD SIGNED

Visualising Chromatin Structure and Dynamics at the Nanometre Scale with Super-Resolution Fluorescence Microscopy

Total Cost €

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EC-Contrib. €

0

Partnership

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 VCSD project word cloud

Explore the words cloud of the VCSD project. It provides you a very rough idea of what is the project "VCSD" about.

metrics    alvarez    gene    biology    srfm    combined    reputation    pluripotent    signal    regulate    classification    noise    cell    expression    lab    marie    labs    central    direct    edge    extensive    innovation    genetic    photonic    organization    utilizes    super    biological    chromatin    determined    thereby    limitations    averaging    remodelling    independent    jason    reinforcing    evident    global    cosma    recently    coupled    time    3d    sciences    dr    characterizing    structure    loza    resolution    altered    cutting    precise    local    demands    first    phd    silencing    host    secondment    body    poor    researcher    otterstrom    types    suited    uniquely    nanoscale    fellow    biophysics    framework    microscopy    mechanisms    fellowship    pluripotency    vcsd    nanometre    overcomes    cells    resolved    therapeutic    dynamics    harvard    correlate    fluorescence    anticipated    restructuring    visualize    biophysical    center    genomic    ensemble    methodology    expert    individual    differentiation    commercializing    poorly    differentiate    spatial    scales    structural    length    expertise    nuclei    pursue    stem    regulation    curie    scientific    supervisor    barcelona   

Project "VCSD" data sheet

The following table provides information about the project.

Coordinator
FUNDACIO INSTITUT DE CIENCIES FOTONIQUES 

Organization address
address: AVINGUDA CARL FRIEDRICH GAUSS 3
city: Castelldefels
postcode: 8860
website: www.icfo.eu

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Spain [ES]
 Total cost 170˙121 €
 EC max contribution 170˙121 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-04-01   to  2018-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO INSTITUT DE CIENCIES FOTONIQUES ES (Castelldefels) coordinator 170˙121.00

Map

 Project objective

Recently, it has become evident that the spatial organization of chromatin within nuclei is a key factor that can regulate gene silencing and expression. This organization is particularly important in pluripotent stem cells that differentiate into all cell types of the body through chromatin remodelling coupled to altered gene expression. Therapeutic use of these cells demands precise control over chromatin structure to direct differentiation. However, chromatin structure remains poorly resolved due to the nanometre length scales involved and limitations of low spatial resolution, poor signal-to-noise and ensemble averaging in existing methods. VCSD utilizes cutting-edge super-resolution fluorescence microscopy (SRFM) that overcomes these limitations. VCSD will, for the first time: 1) visualize global, 3D chromatin nanoscale structure in individual cells during differentiation; and 2) correlate the dynamics of local chromatin restructuring with the silencing of a central pluripotency gene. The proposed Marie Curie Fellow, Jason Otterstrom, PhD Harvard Biophysics, has extensive experience in fluorescence microscopy applied to biological systems. The host lab supervisor, Dr. Loza-Alvarez, is an expert in SRFM, at the Institute for Photonic Sciences, Barcelona. A secondment is planned in the lab of Dr. Cosma, an expert in the genetic mechanisms controlling pluripotency, at the Barcelona Center for Genomic Regulation. The combined expertise of the fellow and host labs is uniquely suited to establish VCSD as a novel framework for characterizing chromatin structure. The methodology developed is anticipated to be adopted by researchers in stem cell and chromatin biology fields, thereby reinforcing Europe’s global reputation in scientific innovation. The Fellowship will enable Jason to pursue applications of the chromatin structural metrics determined here as an independent biophysical researcher, with the long-term goal of commercializing a stem cell classification system.

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