Opendata, web and dolomites

SSINGERG SIGNED

Solid-phase synthesis of imprinted nanoparticles exhibiting glycan epitope recognition in glycoproteins

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 SSINGERG project word cloud

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

behaving    subclasses    combined    polymer    nanoreceptors    incorporated    exhibiting    either    monosaccharides    throughput    data    glass    standalone    limitations    entities    binding    plastic    capacity    glycoproteins    myriad    size    routes    solubility    reactor    diseases    imprinted    sol    combinations    acetylglucosamine    cell    highest    immobilized    prepared    temperature    performance    batch    critical    reproducibility    cope    glycoprotein    optimum    mixture    patentable    column    recognition    automated    synthetic    instrumentation    protocol    antibodies    biology    silica    found    competitive    outputs    protocols    play    criteriously    phases    setting    mixtures    ascertained    immobilization    consisting    mannose    affinity    particles    near    acetylgalactosamine    nanomips    enrichment    nanomip    sorption    glycan    solid    glyproteins    selectivity    isotherm    derive    nanoparticles    subsequent    synthesis    preparation    acetlgalactosamine    filled    monosaccharide    supporting    polymerization    imprinting    receptors    specificity    incubation    glycoproteome    containing    screened    beads    epitope    generate    onto    gel    manner   

Project "SSINGERG" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDADE DO PORTO 

Organization address
address: PRACA GOMES TEIXEIRA
city: PORTO
postcode: 4099 002
website: http://www.up.pt

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 Portugal [PT]
 Total cost 147˙815 €
 EC max contribution 147˙815 € (100%)
 Programme 1. H2020-EU.4. (SPREADING EXCELLENCE AND WIDENING PARTICIPATION)
 Code Call H2020-WF-01-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-10-01   to  2021-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDADE DO PORTO PT (PORTO) coordinator 147˙815.00

Map

 Project objective

The present project aims at the preparation of synthetic nanoreceptors exhibiting glycan epitope recognition in glycoproteins, identified to play a critical role in cell biology and diseases. Such nanoreceptors, behaving like antibodies, may cope with the current limitations in the essential step of enrichment of specific glycan subclasses, within studies of the glycoproteome. The preparation of the receptors will proceed through solid-phase synthesis of imprinted polymer nanoparticles, with the potential to deliver entities with size, specificity and solubility characteristics comparable to antibodies. The solid-phase synthesis of NanoMIP will require the immobilization of important monosaccharides (N-acetylglucosamine, N-acetlgalactosamine, mannose), widely found in glycoproteins, onto supporting beads. Several synthetic routes will be studied for the immobilization onto silica or plastic beads . In a reactor, built as a controlled temperature glass column filled with the beads containing immobilized monosaccharide, criteriously selected polymerization or sol-gel mixtures will generate the nanoMIPs, with subsequent selection of the highest affinity particles. The optimum combinations of solid-phase/imprinting protocol will be screened from a myriad of nanoMIPs prepared in different conditions. The performance of the nanoMIPs will be ascertained by setting a competitive enrichment protocol consisting of the incubation with a mixture of N-acetylglucosamine-, N-acetylgalactosamine- and mannose-containing glyproteins and a non-glycoprotein. Sorption isotherm data will be used to derive important binding features such as capacity, binding affinity and selectivity. Patentable robust solid-phases and imprinting protocols, either in standalone or combined manner, are planned outputs of the project, which may, in the near future, be incorporated into existing automated solid-phase synthesis instrumentation, for increased throughput and batch reproducibility.

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

More projects from the same programme (H2020-EU.4.)

LC-FMRI (2019)

Deciphering the effects of locus coeruleus activity on whole-brain dynamics and neurovascular coupling

Read More  

P-appetite (2019)

Dissecting how the Drosophila brain regulates behavioral sequences of feeding to ensure protein homeostasis

Read More  

ACoDM (2019)

Affective Control of Decision Making

Read More