Explore the words cloud of the BALTIC project. It provides you a very rough idea of what is the project "BALTIC" about.
The following table provides information about the project.
Coordinator |
ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Organization address contact info |
Coordinator Country | Switzerland [CH] |
Total cost | 191˙149 € |
EC max contribution | 191˙149 € (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 2020-06-01 to 2022-05-31 |
Take a look of project's partnership.
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1 | ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE | CH (LAUSANNE) | coordinator | 191˙149.00 |
The cellular life cycle, or cell cycle (CC), is the fundamental backbone of the cellular machinery: it orchestrates processes over multiple scales, in space and time. In bacteria, it consists of an internal clock associated with, for instance, cell-size homeostasis at a population level. Although some analytical tools dedicated to characterizing CC are available for eukaryotic cells, such approaches are still lacking when it comes to bacteria cells study. Moreover, existing eukaryotic cell cyclers are highly limited in terms of both resolution (spatial or temporal) and applications. However, with the rise of antibiotic resistance, there is a real need for reliable quantitative platforms dedicated to bacteria CC and allowing for high throughput comparison studies. This research proposal aims at producing a novel approach for bacteria CC investigation, whilst over-passing the drawbacks associated with existing tools. The developed methodology will rely on cutting edge high throughput super resolution microscopy. We will firstly explore proteins contribution to characterizing CC at the nano-scale, taking a step back from the unreliable and limited size or time dependent estimation. Relying on state of the art machine learning strategies and the identified CC reporting features, I will develop tactics to circumvent the trade-off between temporal and spatial resolution constraining fluorescence nanoscopy when it comes to the study of dynamic processes such as CC. I will implement a methodology to extract, for the first time, dynamic models of bacteria CC from fixed cells super resolved images. It is a considerable step forward: enabling to benefit from a spatial resolution around 10 nm, whilst inferring live-cell akin quantitative information. The highly innovative approaches to bacteria CC quantification developed here will be made generalizable across cell types and applications, providing a unique platform for complex studies, and therapeutics development.
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The information about "BALTIC" are provided by the European Opendata Portal: CORDIS opendata.