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TraffikGene SIGNED

Peptide Dynamic Amphiphiles for Gene Therapy and Macromolecular Delivery

Total Cost €

0

EC-Contrib. €

0

Partnership

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 TraffikGene project word cloud

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

cationic    crossing    scaffolds    connect    vivo    antibody    advantage    alternatives    stakeholders    industrial    decided    dynap    covalent    financial    macromolecular    pegs    cytosolic    platform    therapeutics    health    protection    synthetic    constitute    dynamic    clinical    genetic    mrna    preliminary    peptide    methodology    exogenous    brain    confirms    niches    tools    therapy    oligopeptides    commercial    penetrating    spin    human    vehicles    discoveries    optimize    quick    hydrophobic    alternative    licensing    customized    identification    encouraging    framework    cargo    macromolecules    acids    carefully    glycans    vitro    materials    vectors    blood    aldehyde    erc    nucleic    tails    ipr    off    barrier    traffikgene    market    libraries    diversification    cargos    strategy    rising    polymer    stg    employs    constitutes    diversify    maximized    commercialization    transport    release    gene    cell    bonds    viral    transference   

Project "TraffikGene" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDAD DE SANTIAGO DE COMPOSTELA 

Organization address
address: COLEXIO DE SAN XEROME PRAZA DO OBRADOIRO S/N
city: SANTIAGO DE COMPOSTELA
postcode: 15782
website: http://www.usc.es

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 150˙000 €
 EC max contribution 150˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-PoC
 Funding Scheme ERC-POC
 Starting year 2019
 Duration (year-month-day) from 2019-07-01   to  2020-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDAD DE SANTIAGO DE COMPOSTELA ES (SANTIAGO DE COMPOSTELA) coordinator 150˙000.00

Map

 Project objective

The delivery of exogenous nucleic acids and related macromolecules is one of the most encouraging tools for the future of human health. However, the delivery of the required genetic cargo still constitutes an important challenge. Although non-viral vectors are still in their preliminary clinical steps they are rising up as a real alternative for gene therapeutics. Oligopeptides and polymer cell penetrating materials constitute one of the most promising alternatives for the protection, transport and controlled release of different macromolecular cargos. Under the framework of the ERC-Stg_DYNAP we have methodology that employs dynamic covalent bonds to connect peptide/polymer scaffolds with different aldehyde tails (cationic, hydrophobic, glycans, PEGs, etc.). This key synthetic advantage allows the quick identification of different peptide vehicles for customized cargos. The recent interest of important industrial partners in our technology confirms the strong interest and potential impact of our platform. TraffikGene will diversify the potential market applications of this technology and will allow us to reach a higher level of control for the market transference. We will optimize peptide libraries for the delivery of new nucleic acids (i.e. mRNA) in in vitro and in vivo. The potential commercial success will be maximized by diversification of the applications in gene therapy, cytosolic delivery, antibody transport, cell targeting, blood brain barrier crossing, etc. A market analysis will identify industrial needs, market niches, financial requirements and stakeholders for commercialization. The best future IPR strategy will be carefully evaluated and decided (i.e. product licensing, product development, spin-off, etc.). TraffikGene will allow us to identify and solve challenges required to improve, diversify and exploit the strong potential market applications of our discoveries in the field of gene and macromolecular controlled delivery.

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

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