Opendata, web and dolomites

CasMETICS SIGNED

Combining Single Molecule and Ensemble approaches To Investigate Cas9 Target Search

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 CasMETICS project word cloud

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

perform    dna    assay    hypotheses    bacterial    purified    electroporated    guide    right    infections    determined    quantified    lysis    restriction    nucleic    plan    individual    tagged    atp    hour    tracking    labeled    biological    protection    begin    version    time    unravel    dissociating    double    vitro    fashion    defend       chromosomal    cas9    months    intense    rna    started    molecules    amount    fluorescent    vivo    recognize    o1    experiments    site    bind    molecule    microscopy    directed    crispr    conundrums    fluorescently    laci    critical    single    laco1    dcas9    discover    clock    too    lac    garnered    dsdna    homologous    cleavage    viral    acids    speed    synthetic    mechanistic    enzyme    dye    searching    confer    cells    mysterious       tool    appropriate    binding    fluorescence    biology    rnas    lapse    chromatin    functional    inducer    linked    suggest    stranded    existence    iptg    seem    bsrbi    flowed    immune    cross    search    bulk    melt    recombination   

Project "CasMETICS" data sheet

The following table provides information about the project.

Coordinator
UPPSALA UNIVERSITET 

Organization address
address: VON KRAEMERS ALLE 4
city: UPPSALA
postcode: 751 05
website: www.uu.se

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 Sweden [SE]
 Project website http://elflab.icm.uu.se/
 Total cost 173˙857 €
 EC max contribution 173˙857 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 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    UPPSALA UNIVERSITET SE (UPPSALA) coordinator 173˙857.00

Map

 Project objective

The CRISPR-Cas9 bacterial immune system has garnered intense interest both as a synthetic biology tool and as a biological system in its own right. Yet the ability of Cas9 to find its guide-RNA-directed binding site in a timely fashion remains mysterious. To find its binding site, the single-stranded guide RNA must recognize the appropriate homologous DNA target within double-stranded chromosomal DNA, without using ATP to melt dsDNA. Moreover, in vitro measurements of Cas9 target search seem to suggest that an individual Cas9 molecule should take on the order of months to discover its target site, far too long to defend against viral infections which can proceed to lysis in less than one hour. To begin to unravel these conundrums, I plan to measure Cas9 target search time in vivo, using both single molecule and bulk approaches. The single molecule assay will use fluorescently tagged dCas9 (a version of Cas9 non-functional for cleavage) targeted against the lac O1 binding site. At t=0 the synthetic inducer IPTG can be flowed in, dissociating LacI from the O1 binding site, and the amount of time needed for dCas9 to bind determined by time-lapse fluorescence microscopy. The bulk version of the assay will exploit the existence of a binding site for the restriction enzyme BsrBI in the lacO1 binding site. As in the single molecule assay, the clock is started by addition of IPTG to growing cells, and the time needed for dCas9 binding is quantified by observed how long is needed for dCas9 to confer protection against BsrBI cleavage of cross-linked and purified chromatin. Finally, I will perform high-speed tracking experiments on searching dCas9 molecules using electroporated fluorescent dye-labeled guide RNAs. These measurements should constrain mechanistic hypotheses about Cas9 target search, and may provide insight into other critical biological processes involving single stranded nucleic acids searching in double stranded nucleic acids, such as homologous recombination.

 Publications

year authors and title journal last update
List of publications.
2017 Daniel Lawson Jones, Prune Leroy, Cecilia Unoson, David Fange, Vladimir Ćurić, Michael J. Lawson, Johan Elf
Kinetics of dCas9 target search in Escherichia coli
published pages: 1420-1424, ISSN: 0036-8075, DOI: 10.1126/science.aah7084
Science 357/6358 2019-06-13

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "CASMETICS" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "CASMETICS" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

SSHelectPhagy (2019)

Regulation of Selective autophagy by sulfide through persulfidation of protein targets.

Read More  

ICEDRAGON (2020)

Modelling of dust formation and chemistry in AGB outflows and disks

Read More  

LiverMacRegenCircuit (2020)

Elucidating the role of macrophages in liver regeneration and tissue unit formation

Read More