SMOLDIF

Small-Molecule Probes of Neuronal Differentiation

 Coordinatore Masarykova univerzita 

 Organization address address: Zerotinovo namesti 9
city: BRNO STRED
postcode: 60177

contact info
Titolo: Prof.
Nome: Ctibor
Cognome: Mazal
Email: send email
Telefono: +420 549 495801

 Nazionalità Coordinatore Czech Republic [CZ]
 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-2012-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-11-01   -   2016-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    Masarykova univerzita

 Organization address address: Zerotinovo namesti 9
city: BRNO STRED
postcode: 60177

contact info
Titolo: Prof.
Nome: Ctibor
Cognome: Mazal
Email: send email
Telefono: +420 549 495801

CZ (BRNO STRED) coordinator 100˙000.00

Mappa


 Word cloud

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

cellular    organic    dynamic    scientific    molecule    applicant    molecules    small    neurobiology    neuronal    phenotype    chemical    synthesis    differentiation   

 Obiettivo del progetto (Objective)

'Proposal presented herein combines methods of synthetic organic chemistry, cellular neurobiology, and chemical biology to study processes involved in neuronal differentiation. The primary objective of the project is to discover, characterize, and make broadly available high-quality research tools useful in studies of the dynamic processes of differentiation. The outcome of the project is expected to be of immediate value to the basic research in neurobiology, with potential for clinical applications. To perturb the dynamic process of neuronal differentiation, a small-molecule approach will be pursued. Chemical synthesis will play a central role in providing access to structurally complex molecules that are nontrivial to prepare and, partly as a consequence, underrepresented in the commercial vendor libraries. Ability of the prepared molecules to affect neuronal differentiation will be assessed in phenotype-based assay employing physiologically relevant neuronal cultures. Identification of cellular targets binding to the active small molecules will be an integral part of the project and will make use of small molecule-derived reagents and proteomic analysis. A link between the small-molecule structure, neuronal phenotype, and cellular proteins affected by the small molecule, will be instrumental en route to the small-molecule probes of neuronal differentiation. The multidisciplinary nature of the project necessitates interaction among several laboratories, including the applicant’s laboratory for organic synthesis, in order to realize the objectives of the proposal. Establishment of such research environment will catalyze applicant’s integration into the scientific community of Masaryk University in the Czech Republic and development of lasting scientific connections within the region (“centers of excellence” FNUSA-ICRC and CEITEC) and Europe-wide (Max Planck Institute of Molecular Physiology).'

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