Opendata, web and dolomites

HTS MALDI-TOF MDD SIGNED

MALDI-TOF mass spectrometry metabolite screening assays for drug discovery in human disease

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 HTS MALDI-TOF MDD project word cloud

Explore the words cloud of the HTS MALDI-TOF MDD project. It provides you a very rough idea of what is the project "HTS MALDI-TOF MDD" about.

compare    excellent    track    metabolomics    ingelheim    tissue    mapping    cell    lung    model    provides    stone    profile    fluorescence    industry    final    boehringer    biomarkers    protein    effect    imaging    discovery    biology    ionisation    significantly    precision    germany    surface    metabolites    chemical    protocol    peptide    assisted    simultaneously    fibrotic    limited    quantification    validation    detection    flight    drug    first    label    manner    platform    reported    maldi    corner    vitro    mostly    throughput    mass    fellowship    diverse    time    hts    noise    molecules    spectrometry    assayed    pulmonary    disease    signal    tool    ms    samples    matrix    screen    sections    see    screening    date    drugs    unbiasly    reagent    reproducibility    comprehensibly    possibility    free    metabolic    fibrosis    validated    50    unbiased    assays    small    identification    laser    ht    centric    offers    readouts    pharmaceutical    tof    assay    desorption    substances    explored    cellular   

Project "HTS MALDI-TOF MDD" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF NEWCASTLE UPON TYNE 

Organization address
address: KINGS GATE
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU
website: http://www.ncl.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]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2019
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-04-01   to  2022-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF NEWCASTLE UPON TYNE UK (NEWCASTLE UPON TYNE) coordinator 212˙933.00

Map

 Project objective

Discovery for drug targets is a key step within the process of drug development, and is the corner stone in the pharmaceutical industry. This is mostly achieved by high-throughput screening (HTS) approaches in which a large number of chemical substances are assayed for a specific effect or activity in diverse areas of biology. Mass spectrometry (MS) has become a widely adopted tool in this field as it offers the possibility to simultaneously track molecules in a label-free manner, provides excellent signal to noise, reproducibility, assay precision, and a significantly reduced reagent cost when compared to fluorescence-based assays. Matrix-assisted laser/desorption ionisation time of flight (MALDI-TOF) is the most validated surface ionisation method for HTS approaches, but reported applications of this technology have been limited to in vitro assays with simple readouts and to peptide/protein-centric activity assays. To date, comprehensive and unbiased metabolomics based HTS approaches for cellular assays with MALDI-TOF have not been explored. The objective of this fellowship is to set up a MALDI-TOF based cellular assay for HTS metabolomics drug discovery in order to identify a set of metabolites to screen which will enable us to unbiasly and comprehensibly measure, in a HT manner, how drugs affect different metabolic pathways while simultaneously mapping the metabolic profile of the cell. First, I will develop a robust protocol for the detection, identification, and quantification of ~50 small metabolites for cellular assays. Then, I will apply this protocol to track metabolites in a pulmonary fibrosis cellular model, as well as in fibrotic lung tissue sections using MS imaging. The goal is to compare a disease model with the control to see how drugs are affecting these metabolites, and to see if identified biomarkers can be used to identify disease in tissue samples. As a final validation step, I will implement this platform in Boehringer Ingelheim in Germany.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "HTS MALDI-TOF MDD" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "HTS MALDI-TOF MDD" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

CYBERSECURITY (2018)

Cyber Security Behaviours

Read More  

ROSETTA (2020)

Deciphering the Role of aberrant glycOSylation in the rEsponse to Targeted TherApies for breast cancer

Read More  

LiverMacRegenCircuit (2020)

Elucidating the role of macrophages in liver regeneration and tissue unit formation

Read More