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GLYCONOISE SIGNED

Emergent properties of cell surface glycosylation in cell-cell communication

Total Cost €

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EC-Contrib. €

0

Partnership

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 GLYCONOISE project word cloud

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

biophysical    messaging    dimensional    questions    decoding    covered    rate    quantify    stems    biopolymers    expanded    microparticles    first    vary    glycans    reconstructed    emerge    gives    interactions    structure    dense    function    sciences    noise    instrumentation    provides    message    glycobioinformatics    determined    simplified    formed    interaction    glycan    software    identical    differentiation    glycomes    data    influencing    advancements    cell    expressing    biophysics    codes    model    accessible    transmitter    messages    tolerate    biology    single    mixtures    matrix    receptors    cells    reveals    biological    ultra    genetically    lost    robustness    communication    surface    poorly    adapting    trigger    employ    compositions    immunological    cytometry    redundancy    lectin    competitive    techniques    disturb    replacing    experimental    living    binding    fundamental    constants    combining    cellular    glycosylated    sbquo    receiver    composition    enabled    flow    population   

Project "GLYCONOISE" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: Munich
postcode: 80539
website: www.mpg.de

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 Germany [DE]
 Total cost 1˙499˙813 €
 EC max contribution 1˙499˙813 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-STG
 Funding Scheme ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-02-01   to  2022-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (Munich) coordinator 1˙499˙813.00

Map

Leaflet | Map data © OpenStreetMap contributors, CC-BY-SA, Imagery © Mapbox

 Project objective

The surface of every living cell is covered with a dense matrix of glycans. Its particular composition and structure codes important messages in cell-cell communication, influencing development, differentiation, and immunological processes. The matrix is formed by highly complex biopolymers whose compositions vary from cell to cell, even between genetically identical cells. This gives rise to population noise in cell-cell communication. A second level of noise stems from glycans present on the same cell that disturb the decoding of the message by glycans binding receptors through competitive binding. Glycan-based communication is characterized by a high redundancy of both glycans and their receptors. Thus, noise and redundancy emerge as key properties of glycan-based cell-cell communication, but their extent and function are poorly understood.

By adapting a transmitter-receiver model from communication sciences and combining it with state-of-the-art experimental techniques from biophysics and cell biology, we will address two fundamental questions: What is the role of the redundancy in glycan-based communication? How much ‚noise’ can it tolerate, before the message is lost?

To do so, we first establish a simplified model system for glycan-based communication. Biophysical rate constants are determined for lectin-glycan interactions and expanded to glycosylated microparticles that trigger a biological response in lectin expressing receiver cells. Next, single cell glycomes are reconstructed from ultra-high dimensional flow cytometry data using lectin mixtures enabled by recent advancements in instrumentation and glycobioinformatics software. Glycomes accessible on single cell level allow replacing the microparticles with transmitter cells and employ a cell-cell interaction model. Our transmitter-receiver model is used to quantify the noise and reveals how redundancy provides robustness of messaging by cell surface glycans in cellular communication.

 Publications

year authors and title journal last update
List of publications.
2019 Jessica Schulze, Mareike Rentzsch, Dongyoon Kim, Lydia Bellmann, Patrizia Stoitzner, Christoph Rademacher
A Liposomal Platform for Delivery of a Protein Antigen to Langerin-Expressing Cells
published pages: 2576-2580, ISSN: 0006-2960, DOI: 10.1021/acs.biochem.9b00402
Biochemistry 58/21 2019-10-03

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