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G4invivo SIGNED

Probing intracellular folding and dynamics of telomeric DNA structures with single-molecule FRET

Total Cost €

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EC-Contrib. €

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Partnership

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 G4invivo project word cloud

Explore the words cloud of the G4invivo project. It provides you a very rough idea of what is the project "G4invivo" about.

regulation    life    made    live    accurately    dynamics    anticancer    techniques    decades    versatile    remained    isolated    cell    idea    telomeres    terminating    guanine    distributions    genome    therapies    progress    molecules    folding    chromosomes    linear    physiological    situation    suitable    functions    milieu    drug    single    opportunity    molecular    function    considerable    tandem    ends    telomeric    vital    conformation    dna    maintenance    biophysical    ouml    environments    lack    cellular    integrity    quadruplexes    fret    powerful    measured    inside    combination    adopting    quadruplex    living    bridge    transfer    heterogeneous    efficacy    machines    vitro    consists    optical    technique    describes    individual    biological    limited    investigation    employ    eukaryotic    structures    microscopy    fluorescence    sequences    biology    gap    human    distance    underlying    distances    rster    stranded    stimulate    active    cells    balance    structure    enhancement    energy    resonance    fundamental    perform    mechanistic    molecule    thousands    largely   

Project "G4invivo" data sheet

The following table provides information about the project.

Coordinator
AARHUS UNIVERSITET 

Organization address
address: NORDRE RINGGADE 1
city: AARHUS C
postcode: 8000
website: www.au.dk

contact info
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 Coordinator Country Denmark [DK]
 Project website http://inano.au.dk/about/research-groups/single-molecule-biophotonics-group-victoria-birkedal/people/
 Total cost 212˙194 €
 EC max contribution 212˙194 € (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 2016-01-01   to  2017-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    AARHUS UNIVERSITET DK (AARHUS C) coordinator 212˙194.00

Map

 Project objective

Telomeres, the ends of linear eukaryotic chromosomes, are one of the most versatile “molecular machines” of life. They perform a vital role in several fundamental processes in biology, as maintenance of genome integrity and the regulation of cell growth. Human telomeric DNA consists of thousands of tandem repeats of guanine-rich sequences, terminating the chromosomes. Under physiological conditions, such guanine-rich repeats are capable of adopting four stranded structures, called G-quadruplex DNA. Considerable research has been dedicated to an understanding of functions of telomeres, and during the past decades, much progress has been made towards identifying the underlying processes for G-quadruplex DNA isolated in vitro. However, most of our knowledge of conformation and mechanistic understanding of the balance between the structure and function of telomeric DNA inside cells has remained very limited, largely due to a lack of suitable methods. An opportunity to bridge this gap is single-molecule fluorescence microscopy in combination with Förster resonance energy transfer (FRET), a powerful technique that allows distances, distance distributions, and dynamics of individual biological molecules to be measured even in complex and heterogeneous environments, as cellular milieu. The goal of this project is to employ such optical single-molecule techniques to perform a comprehensive biophysical analysis of the folding and dynamics of G-quadruplex DNA within live cells. This investigation will provide an idea of how accurately our current understanding of the folding and dynamics of G-quadruplex DNA in vitro describes the situation inside the living cell, and will, among other aspects, be crucial for understanding the biological functions of G-quadruplexes and in particular may stimulate the enhancement of the efficacy of the novel anticancer therapies, which use these structures as an active target for drug development.

 Publications

year authors and title journal last update
List of publications.
2017 Andreas Sprengel, Pascal Lill, Pierre Stegemann, Kenny Bravo-Rodriguez, Elisa-C. Schöneweiß, Melisa Merdanovic, Daniel Gudnason, Mikayel Aznauryan, Lisa Gamrad, Stephan Barcikowski, Elsa Sanchez-Garcia, Victoria Birkedal, Christos Gatsogiannis, Michael Ehrmann, Barbara Saccà
Tailored protein encapsulation into a DNA host using geometrically organized supramolecular interactions
published pages: 14472, ISSN: 2041-1723, DOI: 10.1038/ncomms14472
Nature Communications 8 2019-06-18
2016 Mikayel Aznauryan, Siri Søndergaard, Sofie L. Noer, Birgit Schiøtt, Victoria Birkedal
A direct view of the complex multi-pathway folding of telomeric G-quadruplexes
published pages: 11024-11032, ISSN: 0305-1048, DOI: 10.1093/nar/gkw1010
Nucleic Acids Research 44/22 2019-06-18

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