Opendata, web and dolomites

MingleIFT SIGNED

Multi-color and single-molecule fluorescence imaging of intraflagellar transport in the phasmid chemosensory cilia of C. Elegans

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 MingleIFT project word cloud

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

antenna    grasp    length    cilia    phasmid    motors    dynein    interlinked    molecule    waste    regulation    organelles    machinery    moving    trains    antennas    imaging    kinesins    normal    model    individual    soluble    intracellular    eukaryotic    color    effect    building    structure    sensory    specialised    transport    initiating    organism    recycle    blocks    made    understand    chemical    consist    signal    characterised    cellular    complexes    tip    single    core    effectors    adjustments    ciliary    external    intraflagellar    animal    retrograde    elegans    toolbox    sense    signalling    axoneme    mechanistic    dynamics    ift    contacts    proteins    microtubule    membrane    environment    ultimately    template    obtain    outwards    mediate    chemotaxis    water    transducers    discovery    chemosensory    base    tactic    maintenance    connection    subtle    techniques    protrude    cells    protein    cues    cargoes    function    anterograde    components    acting    motor    acts    overarching    encapsulated    turnaround   

Project "MingleIFT" data sheet

The following table provides information about the project.

Coordinator
STICHTING VU 

Organization address
address: DE BOELELAAN 1105
city: AMSTERDAM
postcode: 1081 HV
website: www.vu.nl

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 Netherlands [NL]
 Total cost 175˙572 €
 EC max contribution 175˙572 € (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 2020-03-01   to  2022-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    STICHTING VU NL (AMSTERDAM) coordinator 175˙572.00

Map

 Project objective

Sensory cilia are essential ‘antenna-like’ organelles that protrude out of many eukaryotic cells, acting as signal transducers, enabling cells to sense and respond to the external environment. The model system for this proposed study, chemosensory cilia of C. elegans are well characterised and enable the animal to sense water soluble effectors in the environment for chemotaxis. Cilia consist of an axoneme encapsulated with a signalling protein-rich ciliary membrane. The axoneme, which is a microtubule-based core structure, acts as a template for a specialised intra-cellular transport, intraflagellar transport (IFT). IFT trains are large protein complexes that mediate contacts between motor proteins (IFT kinesins and IFT dynein) and ciliary cargoes, crucial for the formation and maintenance of the cilia, with anterograde IFT trains moving outwards from the ciliary base to deliver ciliary building blocks to the ciliary tip and retrograde IFT trains moving from the ciliary tip to the ciliary base to recycle the waste products. The overarching objective of this project is to grasp the connection between chemosensory function of cilia (initiating chemotaxis), IFT and ciliary length-regulation using single-molecule imaging techniques. In order to achieve this, (i) I will develop a multi-color and single-molecule imaging toolbox to study IFT in the phasmid chemosensory cilia of C. elegans. (ii) Using the toolbox, I will obtain a mechanistic understanding of turnaround dynamics of the IFT machinery (IFT motors and components of the IFT trains), during normal IFT. (iii) A comprehensive understanding of normal IFT will enable discovery of the subtle adjustments made by the IFT machinery, and its effect on the cilia length, in response to chemical cues in the external environment. Ultimately, the goal is to understand how organism level tactic response is interlinked with intracellular transport in the ciliary antennas of individual cells, using C. elegans as a model system.

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

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

VINCI (2020)

The Value of Information and Choice to Improve Control.

Read More  

STIMOS (2019)

Stimulation of Multiple Organoids Simultaneously

Read More  

BirthControlEnvirons (2019)

Contraception meets the environment: everyday contraceptive practices, politics, and futures in a toxic age

Read More