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Identification of therapeutic molecules to target compartmentalised cAMP signalling networks in human disease

Objective

Major diseases including cardiovascular and renal diseases, diabetes mellitus, obesity, diseases of the immune system, cancer and neurological disorders are caused or are associated with disturbances of compartmentalization cAMP signalling networks.
Key players in cAMP signalling are adenylyl cyclases (AC) synthesizing cAMP, phosphodiesterases (PDE) hydrolysing it, and A-kinase anchoring proteins (AKAP) tethering protein kinase A (PKA), the principal effector of cAMP, to cellular compartments. In a multidisciplinary approach based on postgenomic research, we will use established and novel cell lines to identify small 'druggable' therapeutic molecules derived from small molecule libraries which
i.) displace PKA, AKAPs and PDEs from their cognate intracellular location and
ii.) disrupt protein-protein interactions involving ACs, PDEs, AKAPs and PKA in cellular disease models.
The disease models represent cardiovascular diseases, nephrogenic diabetes insipidus (NDI), asthma, chronic obstructive pulmonary disease (COPD), AIDS, obesity, and schizophrenia. Screening of compound libraries will be performed in living cells and in vitro with purified components of the cAMP signalling system. We aim to identify the molecular targets of small molecules using established and to be developed tools and bioassays.
Cell signature responses to challenges with small molecules will be defined in order to gain mechanistic insight into the effects on the disease phenotypes and to anticipate side effects of identified substances. The small molecules will be valuable tools to investigate compartmentalised cAMP signalling. Moreover, this approach may lead to alternative strategies for the treatment of diseases associated with altered cAMP signalling that are not addressed effectively by conventional pharmacotherapy.'

Call for proposal

FP6-2005-LIFESCIHEALTH-6
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Funding Scheme

STREP - Specific Targeted Research Project

Coordinator

FORSCHUNGSVERBUND BERLIN E.V. / FORSCHUNGSINSTITUT FÜR MOLEKULARE PHARMAKOLOGIE
Address
Rudower Chaussee 17
Berlin
Germany

Participants (8)

UNIVERSITAET KASSEL
Germany
Address
Moenchebergstrasse 19
Kassel
UNIVERSITY OF OSLO
Norway
Address
Problemveien 7
Oslo
FONDAZIONE TELETHON
Italy
Address
Via Guglielmo Saliceto 5
Roma
UNIVERSITY OF GLASGOW
United Kingdom
Address
University Avenue
Glasgow
BIAFFIN GMBH & CO KG
Germany
Address
Avz 2, Heinrich-plett-str. 40
Kassel
LAURAS AS
Norway
Address
Gaustadalleen 21
Oslo
BIOLOG LIFE SCIENCE INSTITUTE, FORSCHUNGSLABOR UND BIOCHEMICA-VERTRIEB GMBH
Germany
Address
Flughafendamm 9A
Bremen
GÖTEBORGS UNIVERSITET
Sweden
Address
Vasaparken
Göteborg