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APTAFRAME SIGNED

DNA-origami frame platform for co-evolution ligand selection

Total Cost €

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EC-Contrib. €

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Partnership

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 APTAFRAME project word cloud

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

resolved    structures    em    binding    platform    addressability    epitopes    fragments    discovery    interrogation    libraries    molecular    single    diagnostics    vitro    biotechnology    coverage    affinity    tool    predefined    dna    chain    power    biosensor    accessible    economic    expedites    spatial    generate    aptamers    biomolecules    economaffinity    direct    interactions    cryo    evolution    dimensional    conjunction    structure    reconstruction    scientific    context    combination    antibodies    yielding    avidity    diseases    systematic    generation    lt    toolbox    therapy    co    100kda    transformational    parallel    rational    exploits    ligands    cover    systematically    multidimensional    feedback    provides    reconstructions    once    despite    scfv    paramount    recognition    structural    strategy    origami    complexes    smaller    leveraging    contrast    proteome    tools    antibody    form    electron    cooperative    framework    microscopy    ligand    treatment    reagents    fv    nanotechnology   

Project "APTAFRAME" data sheet

The following table provides information about the project.

Coordinator
UNITED KINGDOM RESEARCH AND INNOVATION 

Organization address
address: POLARIS HOUSE NORTH STAR AVENUE
city: SWINDON
postcode: SN2 1FL
website: n.a.

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 United Kingdom [UK]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-RI
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNITED KINGDOM RESEARCH AND INNOVATION UK (SWINDON) coordinator 212˙933.00

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 Project objective

Affinity reagents such as antibodies and aptamers are of paramount importance as tools in biotechnology and the treatment of a wide range of diseases. However, despite their scientific and economAffinity reagents such as antibodies and aptamers are of paramount importance as tools in biotechnology and the treatment of a wide range of diseases. However, despite their scientific and economic impact it remains challenging to systematically generate high-affinity ligands to cover all epitopes of a given target. Here I propose a strategy to provide spatial control over ligand discovery process leveraging the power of in vitro evolution in conjunction with the spatial addressability of DNA nanotechnology methods. Together they form a new discovery platform for the systematic and parallel generation of ligands, specifically aptamers and single-chain Fv antibody fragments (scFv), to provide coverage of epitopes at predefined targets. The proposed strategy exploits cooperative binding (avidity), by co-evolution of the affinity reagents, in the context of a defined molecular three-dimensional framework provided by DNA origami structures. This further expedites structure determination of ligand-target complexes by cryo-electron microscopy (cryo-EM). The combination of rational framework design, in vitro evolution and structural feedback provided by cryo-EM reconstructions will provide a toolbox for the systematic generation of ligands to all accessible epitopes. Our approach also provides a tool for electron microscopy reconstruction of smaller (< 100kDa) biomolecules and their molecular interactions by enhancing contrast and providing context. Once established, this approach will provide a transformational technology platform that enables the parallel interrogation of multidimensional, spatially resolved libraries, yielding cooperative ligands for highly specific target recognition, with direct applications in biosensor development, proteome analysis, diagnostics and therapy.

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

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