Explore the words cloud of the SWEETOOLS project. It provides you a very rough idea of what is the project "SWEETOOLS" about.
The following table provides information about the project.
Coordinator |
USTAV ORGANICKE CHEMIE A BIOCHEMIE, AV CR, V.V.I.
Organization address contact info |
Coordinator Country | Czech Republic [CZ] |
Total cost | 1˙405˙625 € |
EC max contribution | 1˙405˙625 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2015-STG |
Funding Scheme | ERC-STG |
Starting year | 2016 |
Duration (year-month-day) | from 2016-02-01 to 2021-01-31 |
Take a look of project's partnership.
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1 | USTAV ORGANICKE CHEMIE A BIOCHEMIE, AV CR, V.V.I. | CZ (PRAHA 6) | coordinator | 1˙405˙625.00 |
Glycans are ubiquitous biomolecules found throughout all kingdoms of life. Early studies contributed considerably to our appreciation of glycan functions by showing that abnormalities in the glycosylation can develop into pathogenesis and severe dysfunctions. Despite the crucial role of sugars in many biological events we still do not have adequate tools to decipher their complexity. To unveil the mysteries in the rapidly emerging field of glycobiology we aim in this proposal to develop new tools that will help us to study and understand these important biomolecules. To realize this, we plan to combine the unique targeting capability of biologics with the inhibitory effect of small molecules into robust constructs with advanced properties. The biological part of the construct will be evolved using synthetic peptide libraries ensuring high selectivity toward particular sugar processing enzymes. The second part of the construct will consist of small molecular inhibitor warhead that will be designed and synthesized based on crystal structure-aided analyses. To merge these two moieties we aim to develop a new target enzyme–templated fluorogenic in situ click chemistry methodology that will enable us to easily monitor and screen whole peptide–small molecule bioconjugate libraries as highly selective inhibitors and manipulators of sugar processing enzymes. In addition, we aim to create new multivalent heteroglycosystems by using bioorthogonal reactions on peptide library scaffold. These structures will enable us to study polyvalent carbohydrate–protein interactions and to generate novel therapeutics such as influenza virus entry blockers. Our goal is to develop a new class of smart bioconjugate probes that will help us to answer fundamental questions in glycobiology. The outcomes of this project will significantly deepen our knowledge of glycoconjugates and in the long term, will allow for the design of efficient vaccines and for the development of selective therapeutics.
year | authors and title | journal | last update |
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2019 |
Sebastian Joseph Siegl, Juraj Galeta, Rastislav Dzijak, Arcadio Vázquez, Miguel Del RÃo-Villanueva, Martin DraÄÃnský, Milan Vrabel An extended approach for the development of fluorogenic trans-cyclooctene-tetrazine cycloadditions published pages: , ISSN: 1439-4227, DOI: 10.1002/cbic.201800711 |
ChemBioChem | 2019-04-18 |
2018 |
Sebastian J. Siegl, Arcadio Vázquez, Rastislav Dzijak, Martin DraÄÃnský, Juraj Galeta, Robert Rampmaier, Blanka Klepetářová, Milan Vrabel Design and Synthesis of Aza-Bicyclononene Dienophiles for Rapid Fluorogenic Ligations published pages: 2426-2432, ISSN: 0947-6539, DOI: 10.1002/chem.201705188 |
Chemistry - A European Journal 24/10 | 2019-03-18 |
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The information about "SWEETOOLS" are provided by the European Opendata Portal: CORDIS opendata.