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MACROIMAGING SIGNED

Specific Fluorogenic Peptides for Imaging Metastasis-associated Macrophages

Total Cost €

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EC-Contrib. €

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Partnership

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 MACROIMAGING project word cloud

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

interdisciplinary    fate    innovative    generate    knockouts    mainly    thermodynamics    cohorts    size    reversible    combinatorial    supply    recognition    theranostics    recruitment    enormous    normal    methodology    click    preparation    endocytosis    amplify    fluorogenic    chemistry    reduces    recruited    first    encompassing    selectivity    selective    suggesting    cancer    tools    cell    probes    libraries    fluoromacs    tetrapeptides    macrophages    persistent    showing    vivo    abundant    lack    metastasis    technologies    microenvironment    tm    imaging    technique    cyclic    bonds    cd11b    vitro    fluorophores    cells    elusive    dynamic    drug    report    confirmed    biology    metastatic    disulfide    progress    protein    generation    chemical    dcc    discovery    receptors    localisation    tumours    receptor    metastasing    cuaac    depletion    mediated    tumour    optimisation    governed    affinity    nutshell    understand    individual    populations    conjugation    macroimaging    peptides    macrophage   

Project "MACROIMAGING" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF EDINBURGH 

Organization address
address: OLD COLLEGE, SOUTH BRIDGE
city: EDINBURGH
postcode: EH8 9YL
website: www.ed.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 http://www.dynafluors.co.uk
 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-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-10-01   to  2017-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF EDINBURGH UK (EDINBURGH) coordinator 183˙454.00

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 Project objective

MACROIMAGING is a highly interdisciplinary project encompassing the preparation and optimisation of innovative fluorogenic imaging tools with high selectivity for metastasis-associated macrophages. The metastatic potential of tumours is defined by the tumour microenvironment (TM), where macrophages are the most abundant cells. However, the role of macrophages in the TM remains elusive mainly because of the lack of technologies to target these unique populations of cells in vivo. CD11b metastasis-associated macrophages are recruited by metastasing cancer cells. Their depletion reduces the number and size of metastasis, suggesting that their recruitment is essential for persistent growth of cancer cells. However, there is a need for imaging tools that report the localisation and cell fate of these macrophages to understand how they help tumour cells to progress in the TM. By means of Dynamic Combinatorial Chemistry, libraries of cyclic peptides will be generated from individual tetrapeptides through reversible disulfide bonds. Governed by thermodynamics, DCC will amplify cyclic peptides showing high affinity for CD11b macrophage receptors, involved in the development of metastasis. This technique will supply specific cyclic peptides targeting CD11b. Click chemistry (i.e. CuAAC) will allow the conjugation of these peptides to macrophage-specific fluorophores to generate FLUOROMACS. FLUOROMACS will enable selective imaging of CD11b macrophages by means of receptor-mediated endocytosis. Selectivity will be confirmed in vitro using macrophages from normal cohorts and knockouts. Finally Fluoromacs will be optimised as in vivo imaging probes for metastasis-associated macrophages. In a nutshell, MACROIMAGING will provide the first generation of chemical probes for imaging metastasis-associated macrophages in vivo. This methodology will also have enormous impact in other areas of chemical biology, such as protein recognition, drug discovery and theranostics.

 Publications

year authors and title journal last update
List of publications.
2017 Ramon Subiros-Funosas, Lorena Mendive-Tapia, Jesus Sot, John D. Pound, Nicole Barth, Yaiza Varela, Felix M. Goñi, Margaret Paterson, Christopher D. Gregory, Fernando Albericio, Ian Dransfield, Rodolfo Lavilla, Marc Vendrell
A Trp-BODIPY cyclic peptide for fluorescence labelling of apoptotic bodies
published pages: 945-948, ISSN: 1359-7345, DOI: 10.1039/C6CC07879F
Chem. Commun. 53/5 2019-06-17
2017 Antonio Fernandez, Matthieu Vermeren, Duncan Humphries, Ramon Subiros-Funosas, Nicole Barth, Lara Campana, Alison MacKinnon, Yi Feng, Marc Vendrell
Chemical Modulation of in Vivo Macrophage Function with Subpopulation-Specific Fluorescent Prodrug Conjugates
published pages: 995-1005, ISSN: 2374-7943, DOI: 10.1021/acscentsci.7b00262
ACS Central Science 3/9 2019-06-17
2017 Lorena Mendive-Tapia, Ramon Subiros-Funosas, Can Zhao, Fernando Albericio, Nick D Read, Rodolfo Lavilla, Marc Vendrell
Preparation of a Trp-BODIPY fluorogenic amino acid to label peptides for enhanced live-cell fluorescence imaging
published pages: 1588-1619, ISSN: 1754-2189, DOI: 10.1038/nprot.2017.048
Nature Protocols 12/8 2019-06-17

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