Opendata, web and dolomites

PACEMech TERMINATED

The structure and molecular mechanism of transport proteins within the PACE family of multidrug efflux pumps

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 PACEMech project word cloud

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

membrane    acinetobacter    experts    function    supervisor    bacterial    vision    identification    draw    antibiotics    first    mechanisms    pathogen    molecular    pumps    class    pump    multidrug    resistance    antimicrobial    data    recognised    expertise    cell    export    henderson    lasting    career    founding    actively    human    efflux    structure    details    strategies    transport    describing    combination    reveal    sixth    collaborative    links    laboratory    conducting    proteins    specialised    health    biochemical    hospital    collective    diverse    baumannii    biophysical    drug    biocides    acei    colleagues    structural    conferred    representative    families    paucity    protein    receive    establishing    fellowship    training    mediate    pathogens    regulation    pace    extensively    light    15    mechanism    biophysics    broad    extend    worldwide    family    powerful    fundamental    interfere    genomics    superfamilies    greatest    proteobacterial    classically    vitro    prof    play    overcome    peter    threats    expert    remarkably    compound    collections    functional   

Project "PACEMech" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF LEEDS 

Organization address
address: WOODHOUSE LANE
city: LEEDS
postcode: LS2 9JT
website: www.leeds.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.astbury.leeds.ac.uk/people/staff/staffpage.php
 Total cost 195˙454 €
 EC max contribution 195˙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 2017-01-09   to  2019-01-08

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF LEEDS UK (LEEDS) coordinator 195˙454.00

Map

 Project objective

Antimicrobial resistance is recognised as one of the greatest threats to human health worldwide. Multidrug efflux pumps play a major role in the development of drug resistance in bacterial pathogens. These pumps are able to actively export remarkably broad collections antibiotics and biocides out of the cell. Multidrug efflux pumps have classically been organised into five distinct families or superfamilies. Due to their importance, representative proteins from each of these families have been extensively studied.

Using a combination of functional genomics and biochemical methods to study antimicrobial resistance in the hospital pathogen Acinetobacter baumannii, I recently identified AceI, the founding member of a sixth family of multidrug efflux pumps called the Proteobacterial Antimicrobial Compound Efflux (PACE) family. The PACE family is the first new family of efflux pumps to be described in 15 years. In light of its recent identification, there is a paucity of fundamental data describing how PACE family pumps mediate drug efflux. This proposal will apply in vitro biochemical, biophysical and structural analyses to reveal molecular details of the structure and functional transport mechanism operating in PACE family pumps.

This proposal will draw on the diverse collective expertise of my Fellowship Supervisor Prof Peter Henderson and his expert colleagues in membrane protein structural analyses and biophysics. In conducting this research I will build lasting collaborative links with these experts that will extend beyond the duration of this fellowship. I will receive specialised training in powerful membrane protein analysis methods that are essential to my career goal of establishing a leading research laboratory examining membrane transport proteins, from regulation to molecular mechanisms. My laboratory vision is to develop novel strategies to interfere with drug efflux pump function and so overcome resistance conferred by this important class of proteins.

 Publications

year authors and title journal last update
List of publications.
2018 Karl A. Hassan, Qi Liu, Liam D.H. Elbourne, Irshad Ahmad, David Sharples, Varsha Naidu, Chak Lam Chan, Liping Li, Steven P.D. Harborne, Alaska Pokhrel, Vincent L.G. Postis, Adrian Goldman, Peter J.F. Henderson, Ian T. Paulsen
Pacing across the membrane: the novel PACE family of efflux pumps is widespread in Gram-negative pathogens
published pages: , ISSN: 0923-2508, DOI: 10.1016/j.resmic.2018.01.001
Research in Microbiology 2019-06-13

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "PACEMECH" 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 "PACEMECH" are provided by the European Opendata Portal: CORDIS opendata.

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

LiverMacRegenCircuit (2020)

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

Read More  

HSQG (2020)

Higher Spin Quantum Gravity: Lagrangian Formulations for Higher Spin Gravity and Their Applications

Read More  

CYBERSECURITY (2018)

Cyber Security Behaviours

Read More