Opendata, web and dolomites

FOLDASYNBIO

Bioinspired Nanostructures by Self-assembly of Amphiphilic Non-peptide Helical Foldamers in Aqueous Environment

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 FOLDASYNBIO project word cloud

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

mission    helical    biomimetic    peptide    oligoamides    nanostructures    building    trained    crystallography    alternatively    realization    exist    acquired    possess    rewarding    morphologies    protein    ray    move    tools    primary    predictable    characterization    assemblies    folding    solution    functions    amphiphilic    foldamers    biomaterials    units    structural    chemistry    drug    self    synthesis    appropriate    combination    france    milestone    natural    oligomers    architectures    folded    secondment    pioneered    group    precisely    catalysts    engineering    biological    synthetic    sequence    structure    patterns    functional    precise    sophistication    bode    resides    techniques    manipulation    potentially    he    advantages    laboratory    construction    quaternary    assembling    join    endeavor    aqueous    secondary    arrangements    multidisciplinary    nanometer    rules    modularity    peptides    foldamer    urea    host    expertise    prominent    difficulty   

Project "FOLDASYNBIO" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITE DE BORDEAUX 

Organization address
address: PLACE PEY BERLAND 35
city: BORDEAUX
postcode: 33000
website: www.nouvelle-univ-bordeaux.fr

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 France [FR]
 Total cost 185˙076 €
 EC max contribution 185˙076 € (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 2015
 Duration (year-month-day) from 2015-09-01   to  2018-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITE DE BORDEAUX FR (BORDEAUX) coordinator 185˙076.00

Map

 Project objective

The design and precise construction of biomimetic self-assembling systems in aqueous solution is a challenging yet potentially highly rewarding endeavor, contributing to the development of new biomaterials, catalysts, drug-delivery systems and tools for the manipulation of biological processes. A high level of sophistication with control over morphologies and functions has been achieved by engineering self-assembling peptide-based building units. Although peptides possess a number of specific advantages including synthetic availability, modularity, one difficulty resides in precisely controlling the rules relating primary sequence and secondary structure. Alternatively, opportunities exist to develop bottom-up approaches using non-natural oligomers also referred to as foldamers, with predictable and well-defined folding patterns. Advances in foldamer chemistry bode well for their use as building units for the precise construction of nanometer scale assemblies and for possible applications. This project will move a step forward towards the realization of this mission, by developing protein-like quaternary arrangements under sequence based control using amphiphilic helical foldamers in aqueous conditions. The applicant has been trained in the synthesis of folded oligoamides and more importantly has acquired a high level of expertise in the design and structural characterization of peptide-based assemblies. He will join and bring his expertise to a host laboratory in France that has pioneered the development of urea-based helical foldamers. Secondment in one established European group with prominent expertise in X-ray crystallography techniques and biological structure determination will provide the appropriate combination of knowledge required for this multidisciplinary study. This approach will be a milestone in the design of foldamer-based quaternary architectures and may lead to new functional nanostructures.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "FOLDASYNBIO" 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 "FOLDASYNBIO" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

MITafterVIT (2020)

Unravelling maintenance mechanisms of immune tolerance after termination of venom immunotherapy by means of clonal mast cell diseases

Read More  

MCRD (2020)

Development Of Microfluidic Based Low Cost Industrial Cryo-Ready Devices For Preservation Of Living Cells

Read More  

TOPOCIRCUS (2019)

Simulations of Topological Phases in Superconducting Circuits

Read More