GLYCAT

Glycosylation Catalysts

 Coordinatore UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN 

 Organization address address: BELFIELD
city: DUBLIN
postcode: 4

contact info
Titolo: Mr.
Nome: Donal
Cognome: Doolan
Email: send email
Telefono: +353 1 7161656
Fax: +353 1 7161216

 Nazionalità Coordinatore Ireland [IE]
 Totale costo 81˙250 €
 EC contributo 81˙250 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2012-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-04-01   -   2016-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN

 Organization address address: BELFIELD
city: DUBLIN
postcode: 4

contact info
Titolo: Mr.
Nome: Donal
Cognome: Doolan
Email: send email
Telefono: +353 1 7161656
Fax: +353 1 7161216

IE (DUBLIN) coordinator 81˙250.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

significant    permutations    synthesise    glycosylations    oligosaccharides    impact    oligopeptides    biology    diseases    stereoselective    oligonucleotides    carbohydrates    linear   

 Obiettivo del progetto (Objective)

'Catalysts for stereoselective glycosylations will be developed. The focus being on designing organocatalysts for catalyst-controlled glycosylations.

Carbohydrates, the most abundant biomolecules on Earth, are intimately involved in many crucial biological processes (signal transduction, cell recognition) and in diseases (AIDS, cancer). They are useful for the investigation of diseases, and have great potential as vaccines and therapeutics. The biology depends on the specific identity (including stereochemistry) of the carbohydrates (usually oligosaccharides – several monosaccharides joined together).

A significant bottleneck in making scientific progress in the strategically important field of glycoscience is the effort and expense required to synthesise pure oligosaccharides and glycoconjugates as single stereochemical isomers. A major synthetic difficulty with oligosaccharides (vs. oligonucleotides or oligopeptides) is the diversity that can exist: a rough calculation suggests that there are ~256 DNA tetranucleotides, ~160,000 tetrapeptides and >4x10^7 linear tetrasaccharides. Added permutations arise from the variety of monosaccharide stereoisomers and the different connectivities possible at each linkage. Many oligosacchardies are not linear but branched - adding further permutations.

Given the impact of the ability to easily synthesise oligopeptides and oligonucleotides have had on modern biology, it is difficult to predict the impact of technology that would allow oligosaccharides to be synthesised with similar ease, other than that it would be highly significant. The proposal seeks to work towards this goal in a way that is complementary to approaches currently being used. Over the past 30 years stereoselective catalysis has transformed the availability of chiral molecules in enantiopure form. However, it has yet to make a similar impact on carbohydrate chemistry. GlyCat will be at the forefront of efforts to change the status quo in saccharide synthesis.'

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