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Bioisotopes TERMINATED

Biological Effects on Isotopically Evaluated Systems

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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Project "Bioisotopes" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITEIT GENT 

Organization address
address: SINT PIETERSNIEUWSTRAAT 25
city: GENT
postcode: 9000
website: http://www.ugent.be

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 Belgium [BE]
 Total cost 160˙800 €
 EC max contribution 160˙800 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-02-01   to  2019-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITEIT GENT BE (GENT) coordinator 160˙800.00

Map

 Project objective

Reliable and robust methods for determining iron, zinc and copper status in the general population are needed. High precision natural intrinsic isotopic techniques originating in Earth Sciences can be used to reveal elusive metal pathways. The tight energy controls in biological systems mean that the isotope effect is seen in different metal-protein environments, depending on the ligand coordination and, if relevant, the oxidation state of the metal. When metal pathways adjust, due to increased or decreased uptake, excretion or another metabolic change, the isotope composition of a metal reservoir reflects this. Recent studies have indicated that these high precision isotopic analyses of blood may provide a new reliable method to determine metal status and disease. However, the interpretation of high precision isotopic data currently relies on computational models and plant-based laboratory experiments, and these assumptions are not sufficient to constrain isotopic signatures in human biological systems. Accurate interpretation of the isotopic signature is key to understanding the metabolic pathway that lead to a change in metal status. This study will investigate the isotopic fractionation of iron, copper and zinc on binding with proteins in simple to complex biological systems, and how this relates to metal cell metabolism, with the key aim of establishing a robust reference frame for future investigations of isotope biochemistry.

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The information about "BIOISOTOPES" are provided by the European Opendata Portal: CORDIS opendata.

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