FP6Reintegration grant2005–2006

METALLOPROTEIN · Interaction of toxic organotin compounds towards human metallothionein-3

FP6 — Marie Curie Actions (Human Resources and Mobility)

Duration
2005-08-01 → 2006-07-31
EU contribution
€40,000
Participants
1
Scheme
ERG

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Results in brief

Final Activity Report Summary - METALLOPROTEIN (Interaction of toxic organotin compounds towards human metallothionein-3)

Metallothioneins (MTs) are low-molecular-weight metalloproteins (MPs) with high cysteine (Cys) content. They are involved in a wide range of biochemical processes. In human MT-1 and MT-2 isoforms are found in all organs, whereas MT-3 is expressed mainly in the brain, known also as growth inhibitory factor (GIF). Human exposure to organotin compounds (OTs) stems from their use as polyvinyl chloride heat stabilisers and as marine biocides. Certain OTs have already been detected in blood, liver or urine samples from individuals. Acute exposures can result in either neurotoxicity or immunotoxicity depending on the specific compound involved. Attention has been focused on the biological chemistry of OTs recently. It has been shown, that Cys is one of the primary biological ligands for OTs. Regarding to its high Cys content, it is likely that main target of OTs in brain cells is MT-3. The objective of this project is to study the interaction of human MT-3 towards neuro- and immunotoxic OTs has been detected in drinking water and in human organism.

Data: CORDIS, © European Union

Project objective

Metallothioneins (MTs) are low-molecular-weight metalloproteins (MPs) with high cysteine (Cys) content. They are involved in a wide range of biochemical processes. In human MT-1 and MT-2 isoforms are found in all organs, whereas MT-3 is expressed mainly in the brain. Human exposure to organotin compounds (OTs) stems from their use as polyvinyl chloride heat stabilizers and as marine biocides. Certain OTs have already been detected in blood, liver or urine samples from individuals. Acute exposures can result in either neurotoxicity or immunotoxicity depending on the specific compound involved. Recently, attention has been focused on the biological chemistry of OTs. It has been shown, that Cys is one of the primary biological ligands for OTs. Regarding to its high Cys content, it is likely that main target of OTs in brain cells is MT-3.The objective of this project is to study the interaction of human MT-3 towards four neuro- and immunotoxic OTs detected in drinking water and in biological samples from human b ody. The conditions of the over-expression, purification and the conversion to an air-stable derivative of recombinant MT-3 will be optimised first. Incorporation of OTs into MTs, composition of the resulting new MP(s) will be studied by electrospray ionisation mass spectrometry (ESI MS), inductively coupled plasma atom emission spectrometry (ICP AES), circular dicroism (CD) and ultraviolet-visible (UV-Vis) spectrophotometry. The incorporation of OTs into Zn-MT-3 under physiological conditions will also be studied. Finally, the inductive effect of OTs on the over-expression of MT-3 will be monitored as a control.

Original text from CORDIS.

Participants

  • UNIVERSITY OF SZEGED · SZEGEDCoordinatorCity levelHungary

Links

Data: CORDIS, © European Union