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.

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

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.)

LYSOKIN (2020)

Architecture and regulation of PI3KC2β lipid kinase complex for nutrient signaling at the lysosome

Read More  

INFANTPATTERNS (2019)

Development of kinematic and muscle patterns in preterm infants

Read More  

EcoSpy (2018)

Leveraging the potential of historical spy satellite photography for ecology and conservation

Read More