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MMXVI

Minimal Model for Pox-Virus Infection

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 MMXVI project word cloud

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

em    hundreds    architecture    protein    viral    function    ing    applicable    diseases    initially    architectural    contact    economic    nanometers    trade    model    poxvirus    first    minimal    infectious    inevitable    super    global    generation    structure    broadly    infection    travel    until    limited    deadly    therapeutic    viruses    structures    membrane    capture    visualization    biological    virus    single    thereby    create    dynamic    biology    analytical    unprecedented    outlined    resolution    lifecycle    tools    microscopy    specificity    complexity    averaging    dynamics    nanoscale    resolutions    highest    tens    investigation    stages    looks    socio    relationships    shifting    prototypic    srm    virion    host    biophysical    world    cell    molecular    precise    events    vectors    burdens    imaging    climate    models    diagnostic    combining    vaccinia    particles    molecule    blebs    capacity    emergence    affords    techniques    initial    structural    nano    amenable    insights   

Project "MMXVI" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY COLLEGE LONDON 

Organization address
address: GOWER STREET
city: LONDON
postcode: WC1E 6BT
website: n.a.

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.ucl.ac.uk/lmcb/users/david-albrecht-0
 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-2016
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-06-01   to  2019-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE LONDON UK (LONDON) coordinator 183˙454.00

Map

 Project objective

Viral diseases represent one of the world’s highest socio-economic burdens. Increased global trade and travel, climate change resulting in shifting viral vectors, and the emergence of new and often deadly viruses is inevitable. Therefore, detailed understanding of the complexity of virus particles and the development of new model systems to study them, will be essential to develop new research, diagnostic, and therapeutic tools. The structural changes that occur during the initial contact between a virus and its host remains one of the major challenges in infection biology. Until recently, the investigation of viral nano-architecture and dynamic changes that occur in virus particles during the infectious lifecycle was limited to methods, such as EM, with no capacity to capture dynamic events or define molecular specificity. The goal of the proposed project is to create a new minimal model of virus infection based on cell-derived membrane blebs. The model will be amenable to novel super-resolution microscopy (SRM) methods that allow the visualization of viral structures at resolutions of tens of nanometers. Recently developed analytical tools like single-virion averaging allows the generation of precise models from hundreds of events. This affords unprecedented insights into the biological and biophysical requirements of virus infection. Furthermore, we aim to investigate the dynamics of virus architectural changes during the first stages of infection, particularly at the membrane level, by combining single-molecule techniques with our new model-system. While initially aimed at investigating protein structure-function relationships within the prototypic poxvirus, vaccinia, the model system and imaging developments outlined will be broadly applicable to a wide range of biological systems including other viruses. Thereby, this proposal looks to advance the field of infection biology into the nanoscale.

 Publications

year authors and title journal last update
List of publications.
2019 Alexander Balinovic, David Albrecht, Ulrike Endesfelder
Spectrally red-shifted fluorescent fiducial markers for optimal drift correction in localization microscopy
published pages: 204002, ISSN: 0022-3727, DOI: 10.1088/1361-6463/ab0862
Journal of Physics D: Applied Physics 52/20 2019-10-31
2019 Robert D. M. Gray, David Albrecht, Corina Beerli, Moona Huttunen, Gary H. Cohen, Ian J. White, Jemima J. Burden, Ricardo Henriques, Jason Mercer
Nanoscale polarization of the entry fusion complex of vaccinia virus drives efficient fusion
published pages: N/A, ISSN: 2058-5276, DOI: 10.1038/s41564-019-0488-4
Nature Microbiology N/A 2019-10-31
2018 Siân Culley, David Albrecht, Caron Jacobs, Pedro Matos Pereira, Christophe Leterrier, Jason Mercer, Ricardo Henriques
Quantitative mapping and minimization of super-resolution optical imaging artifacts
published pages: 263-266, ISSN: 1548-7091, DOI: 10.1038/nmeth.4605
Nature Methods 15/4 2019-10-31
2019 Romain F Laine, Kalina L Tosheva, Nils Gustafsson, Robert D M Gray, Pedro Almada, David Albrecht, Gabriel T Risa, Fredrik Hurtig, Ann-Christin Lindås, Buzz Baum, Jason Mercer, Christophe Leterrier, Pedro M Pereira, Siân Culley, Ricardo Henriques
NanoJ: a high-performance open-source super-resolution microscopy toolbox
published pages: 163001, ISSN: 0022-3727, DOI: 10.1088/1361-6463/ab0261
Journal of Physics D: Applied Physics 52/16 2019-10-31
2019 Pedro M. Pereira, David Albrecht, Siân Culley, Caron Jacobs, Mark Marsh, Jason Mercer, Ricardo Henriques
Fix Your Membrane Receptor Imaging: Actin Cytoskeleton and CD4 Membrane Organization Disruption by Chemical Fixation
published pages: 675, ISSN: 1664-3224, DOI: 10.3389/fimmu.2019.00675
Frontiers in Immunology 10 2019-10-31

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