BIGR | Biophysical Models of Bacterial Growth

Summary
Biology operates in a dynamic, changing environment, with fluctuations occurring over many time and length scales. Microorganisms are capable of duplicating themselves accurately over a short time in this noisy environment. This self-replication, known as the “cell cycle”, must be tightly regulated in order for replication to be efficient. Key processes such as growth (both of volume and biomass), division and DNA replication must be coordinated. What biophysical cues are measured by the cell and what feedback is utilized to achieve this tight control is a fundamental, open and inherently interdisciplinary question. The goal of this proposal is to build integrated models which can account for the simultaneous regulation of multiple cellular traits, and account, quantitatively, for the coupling between the various cellular processes. We will consider coarse-grained models that operate both on long timescales – the coupling of DNA replication, gene expression and cell division – and short timescales, associated with water flow and ion transport across the membrane. Building on our expertise in the physics of stochastic processes, we will develop biophysical models that explain how microbes deal with fluctuations. We will develop new analysis tools that will enable us to learn from fluctuations, in particular through the powerful methodology of causal inference, which has not been previously applied in this context. The models will allow us to study the implications of variability on the population growth and fitness, and elucidate the design principles involved. Taken together, these models will take us toward comprehensive and predictive biophysical models of bacterial growth.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/101125981
Start date: 01-12-2023
End date: 30-11-2028
Total budget - Public funding: 1 708 613,00 Euro - 1 708 613,00 Euro
Cordis data

Original description

Biology operates in a dynamic, changing environment, with fluctuations occurring over many time and length scales. Microorganisms are capable of duplicating themselves accurately over a short time in this noisy environment. This self-replication, known as the “cell cycle”, must be tightly regulated in order for replication to be efficient. Key processes such as growth (both of volume and biomass), division and DNA replication must be coordinated. What biophysical cues are measured by the cell and what feedback is utilized to achieve this tight control is a fundamental, open and inherently interdisciplinary question. The goal of this proposal is to build integrated models which can account for the simultaneous regulation of multiple cellular traits, and account, quantitatively, for the coupling between the various cellular processes. We will consider coarse-grained models that operate both on long timescales – the coupling of DNA replication, gene expression and cell division – and short timescales, associated with water flow and ion transport across the membrane. Building on our expertise in the physics of stochastic processes, we will develop biophysical models that explain how microbes deal with fluctuations. We will develop new analysis tools that will enable us to learn from fluctuations, in particular through the powerful methodology of causal inference, which has not been previously applied in this context. The models will allow us to study the implications of variability on the population growth and fitness, and elucidate the design principles involved. Taken together, these models will take us toward comprehensive and predictive biophysical models of bacterial growth.

Status

SIGNED

Call topic

ERC-2023-COG

Update Date

12-03-2024
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Horizon Europe
HORIZON.1 Excellent Science
HORIZON.1.1 European Research Council (ERC)
HORIZON.1.1.0 Cross-cutting call topics
ERC-2023-COG ERC CONSOLIDATOR GRANTS
HORIZON.1.1.1 Frontier science
ERC-2023-COG ERC CONSOLIDATOR GRANTS