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.

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

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.)

DEF2DEV (2019)

Identification of the mode of action of plant defensins during root development and plant defense responses.

Read More  

RipGEESE (2020)

Identifying the ripples of gene regulation evolution in the evolution of gene sequences to determine when animal nervous systems evolved

Read More  

GrowthDevStability (2020)

Characterization of the developmental mechanisms ensuring a robust symmetrical growth in the bilateral model organism Drosophila melanogaster

Read More