ITCSCEN

Binuclear Non-Coupled Copper Enzymes in Neurobiology: An Integrated Computational/Spectroscopic Investigation

 Coordinatore UNIVERSITY OF NORTHUMBRIA AT NEWCASTLE. 

 Organization address address: "Ellison Place, Ellison Building"
city: NEWCASTLE UPON TYNE
postcode: NE1 8ST

contact info
Titolo: Prof.
Nome: Gary
Cognome: Black
Email: send email
Telefono: +44 191 2273550
Fax: +44 191 2273519

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 258˙386 €
 EC contributo 258˙386 €
 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-2010-IOF
 Funding Scheme MC-IOF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-05-16   -   2014-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY OF NORTHUMBRIA AT NEWCASTLE.

 Organization address address: "Ellison Place, Ellison Building"
city: NEWCASTLE UPON TYNE
postcode: NE1 8ST

contact info
Titolo: Prof.
Nome: Gary
Cognome: Black
Email: send email
Telefono: +44 191 2273550
Fax: +44 191 2273519

UK (NEWCASTLE UPON TYNE) coordinator 258˙386.80

Mappa


 Word cloud

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

disorders    enzymes    drugs    nervous    crucial    cu    protein    mechanism   

 Obiettivo del progetto (Objective)

'Every third protein contains metal as cofactor. Cu-enzymes plays crucial rules in key processes in bioenergetics, mitochondrial respiration, neurotransmitter biosynthesis, antioxidation and pigmentation Therefore they are intensive targets for discovering new drugs and the understanding of their structure-functions relationships will provide new insight in translational and biomedical research. In this Marie Curie International Outgoing Fellowship I will investigate the mechanism of important two bi nuclear cupper enzyme – Peptidylglycine α-Amidating Monooxygenase (PAM) and Dopamine β-Monooxygense (DBM) which catalyze hydroxylation of substrates in crucial importance for neurobiology . The miss functionalities of these enzymes are related with nervous system disorders therefore revealing it mechanism will provide advanced opportunities for design of new drugs. In order to achieve this knowledge we will apply integrated combination of the most advanced spectroscopic techniques and state of the art computational methods.'

Introduzione (Teaser)

Scientists have shed light on the mechanisms of function of two important copper (Cu)-containing enzymes involved in nervous system disorders. Increased understanding should lead to advances in drug design, protein engineering and biotechnology.

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