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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.

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

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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