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PIM PROTEOMICS

Unravelling PIM kinase signal integration in the T cell response

Total Cost €

EC-Contrib. €

Partnership

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Outcomes and
results

PIM PROTEOMICS project word cloud

Explore the words cloud of the PIM PROTEOMICS project. It provides you a very rough idea of what is the project "PIM PROTEOMICS" about.

protein regulated context immunotherapy cancer family parallel activated cutting combine independent signals mtor networks quantitative co survival cells manipulated ordinated combinations differentiation signalling outcomes alternative understanding synthesis kinase cell substrates division rational downstream quantify pim integration regulate edge signal immune regulates proteomic quantitatively mathematical immunomodulatory interact regulators diverge integrate critical molecule strength culture qualitatively therapies fundamental fate exploration

Project "PIM PROTEOMICS" data sheet

The following table provides information about the project.

Coordinator	UNIVERSITY OF DUNDEE Organization address address: Nethergate city: DUNDEE postcode: DD1 4HN website: www.dundee.ac.uk contact info title: n.a. name: n.a. surname: n.a. function: n.a. email: n.a. telephone: n.a. fax: n.a.
Coordinator Country	United Kingdom [UK]
Project website	https://www.dundee.ac.uk/research/informationforresearchers/resources/fellowships/marie-curie-fellowship/
Total cost	183˙454 €
EC max contribution	183˙454 € (100%)
Programme	1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
Code Call	H2020-MSCA-IF-2015
Funding Scheme	MSCA-IF-EF-ST
Starting year	2017
Duration (year-month-day)	from 2017-07-01 to 2019-07-13

Partnership

Take a look of project's partnership.

#	participants	country	role	EC contrib. [€]
1	UNIVERSITY OF DUNDEE UNIVERSITY OF DUNDEE Organization address address: Nethergate city: DUNDEE postcode: DD1 4HN website: www.dundee.ac.uk contact info title: n.a. name: n.a. surname: n.a. function: n.a. email: n.a. telephone: n.a. fax: n.a.	UK (DUNDEE)	coordinator	183˙454.00

Map

Project objective

Understanding how T cells integrate alternative signal combinations to determine immune response strength and functionality is of critical importance for rational design of immunomodulatory therapies. The PIM kinase family have been identified as important regulators of cell division, survival and protein synthesis independent of, but in parallel to the key signalling molecule mTOR. I propose to use cutting-edge quantitative proteomic technology to identify substrates and downstream protein networks regulated by PIM kinase in activated T cells. I will investigate where these downstream targets qualitatively diverge from, or quantitatively interact with, the mTOR signalling pathway (Objective 1 and 2). Using advanced cell culture and mathematical modelling I will quantify how this co-ordinated activity regulates T cell division, survival and differentiation outcomes (Objective 3). This comprehensive exploration of PIM kinase and mTOR signalling pathway integration will provide important fundamental insight into how these signals combine to regulate T cell fate and may be manipulated in the context of immunotherapy or cancer.

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