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A system view on the differential activities of human type I interferons

Objective

Type I interferons (IFNs) form a restricted network of highly related immune cytokines that elicit differential biological responses through a single cell surface receptor comprised of the subunits IFNAR1 and IFNAR2. We have shown that differential signal activation correlates with differential interaction and conformational dynamics of the receptor induced by binding of different member of the IFN family. The goal of this project is to employ a systems biology approach to identify the molecular and cellular mechanisms responsible for translating receptor dynamics into differential cellular responses by combining biochemical, biophysical and genetic analysis of the signaling outputs. We will collect quantitative data describing type I interferon signaling from ligand recognition until phenomenological cellular responses in a number of well defined cell lines. Based on detailed structure functions studies, we will generate a set of IFN mutants with highly differential cellular responses. Based on this sub-family of ligands, we will explore the molecular and cellular dynamics of the signaling complex on the plasma membrane, as well as the receptor trafficking upon activation. Moreover, we will analyze the protein-protein interaction network involved in signal transduction and obtain a spatio-temporal picture of key signaling pathways. These studies will be flanked by extensive analyses of gene transcription levels and correlated with cellular responses. Using these data sets, input and output signals will be correlated on different levels by various mathematical approaches to understand how the processing of differential input signals is translated within the cell to produce different responses to binding the same surface receptors. In order to test the validity of these models, experimental and theoretical studies will be tightly coupled, for example, in designing network perturbations. As a proof-of-concept for this approach, we will design IFNs with optimized potencies for medical application, such as the ex vivo differentiation of monocytes into dendritic cell for application as cancer vaccines.

Call for proposal

FP7-HEALTH-2007-B
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Coordinator

UNIVERSITAET OSNABRUECK
Address
Neuer Graben/schloss 29
49074 Osnabrueck
Germany
Activity type
Higher or Secondary Education Establishments
EU contribution
€ 773 560
Administrative Contact
Renate Sokolowski (Ms.)

Participants (4)

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
France
EU contribution
€ 570 977
Address
Rue Michel Ange 3
75794 Paris
Activity type
Other
Administrative Contact
Jean-Michel Portefaix (Mr.)
WEIZMANN INSTITUTE OF SCIENCE
Israel
EU contribution
€ 540 180
Address
Herzl Street 234
7610001 Rehovot
Activity type
Higher or Secondary Education Establishments
Administrative Contact
Talia Tzahor (Ms.)
INSTITUT PASTEUR
France
EU contribution
€ 472 000
Address
Rue Du Docteur Roux 25-28
75724 Paris Cedex 15
Activity type
Research Organisations
Administrative Contact
Nadia Khelef (Dr.)
EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH
Switzerland
EU contribution
€ 509 688
Address
Raemistrasse 101
8092 Zuerich
Activity type
Higher or Secondary Education Establishments
Administrative Contact
Jörg Stelling (Prof.)