GPCR-LGIC COUPLING

Interactions between G-protein Coupled Receptors and Ligand Gated Ion Channels

 Coordinatore MIDDLE EAST TECHNICAL UNIVERSITY 

 Organization address address: DUMLUPINAR BULVARI 1
city: ANKARA
postcode: 6800

contact info
Titolo: Dr.
Nome: ?rem
Cognome: Dikmen Toker
Email: send email
Telefono: 903122000000
Fax: 903122000000

 Nazionalità Coordinatore Turkey [TR]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 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-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-10-01   -   2014-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    MIDDLE EAST TECHNICAL UNIVERSITY

 Organization address address: DUMLUPINAR BULVARI 1
city: ANKARA
postcode: 6800

contact info
Titolo: Dr.
Nome: ?rem
Cognome: Dikmen Toker
Email: send email
Telefono: 903122000000
Fax: 903122000000

TR (ANKARA) coordinator 100˙000.00

Mappa


 Word cloud

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

drugs    receptor    dopamine    interactions    adenosine    channels    cell    model    live    reveal    neurological    molecular    trimeric    fluorescence    receptors    dopaminergic    nmda    schizophrenia    protein    technique    coupled    ion    regulation   

 Obiettivo del progetto (Objective)

'Dopamine receptors are members of G-protein coupled receptor superfamily. These receptors are the key point of dopaminergic system, which controls the regulation of memory, attention, food intake, endocrine regulation, psychomotor activity and positive reinforcement. To regulate so many critically important neurological events, dopamine receptors have complex interactions with other receptors and ion channels. In this study, a trimeric complex comprising D2 receptor -which is a subtype of dopamine receptors- , A2A adenosine receptor being another G-protein coupled receptor and a ligand gated ion channel N-methyl-D-aspartate (NMDA) receptor will be investigated. The aim of this project will be the application of a novel technique we refer as SplitGFP-FRET for the first time. For this study, “Fluorescence Resonance Energy Transfer” and “Split GFP” methods will be combined so as to reveal the trimeric D2 dopamine receptor- A2A adenosine receptor-NMDA receptor interactions. With the proposed study, a fluorescence technique to analyze live cell culture will be developed. This model will potentially lead to understanding of molecular mechanisms of many neuropathological conditions like schizophrenia and Parkinson’s disease because these disorders have already been shown to be associated with dysregulations in dopaminergic systems. Therefore, this project aims to reveal detailed links between schizophrenia and interactions of D2 dopamine receptor with other receptors and ion channels. The developed live cell model will also be useful for testing anti-psychotic drugs whether they have effects on disruption of protein-protein interactions, which will, in turn, ease screening of newly designed drugs.'

Introduzione (Teaser)

A new imaging approach developed by EU-funded researchers should help provide the much-awaited molecular evidence behind neurological conditions.

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