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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.

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

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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