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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.

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

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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