Summary
Many bacteria possess a paracrystaline protein coat named the S-layer. S-layers cover the entire cell surface and are involved in protection, virulence, cell-shape maintenance and communication. Lattice integrity is essential for S-layer function, meaning that its assembly must be intimately coordinated with cell growth and division. Some studies have reported that S-layer biogenesis co-localizes with peptidoglycan (PG) synthesis, however, the underlying molecular mechanisms remain unknown. Here, I will investigate the molecular regulatory network that orchestrates S-layer assembly, cell division and PG synthesis in the human pathogen Bacillus anthracis, where S-layer defects render the bacterium avirulent, making this ultrastructure an attractive therapeutic target.
In the SLYDIV project I will 1) structurally and functionally compare Sap and EA1, the exponential and stationary phase S-layer proteins of B. anthracis 2) follow their in vivo assembly using time-resolved labelling and fluorescent microscopy and 3) uncovering the molecular interactions that couple S-layer assembly with the PG and/or cell division machinery. I will make use of chemicals that selectively target the cell cycle or cell division and monitor localization of S-layer assembly, will use nanobodies that disturb S-layer integrity and monitor the localization of cell wall synthesis, and use my interactomics experience to discover contact partners of S-layer and PG synthesis. Thus, SLYDIV is a multidisciplinary and integrative project that combines structural biology, biophysics, cell imaging, and microbiology. In addition, SLYDIV meets my solid knowledge on bacterial cell division with the host labs’ expertise on S-layer structure and function.
The SLYDIV project aims to lead to a major breakthrough in the basic understanding of the regulation of the bacterial cell envelope, while it will pave the way for specific novel molecular therapies against B. Anthracis, a Category A bioterrorist agent.
In the SLYDIV project I will 1) structurally and functionally compare Sap and EA1, the exponential and stationary phase S-layer proteins of B. anthracis 2) follow their in vivo assembly using time-resolved labelling and fluorescent microscopy and 3) uncovering the molecular interactions that couple S-layer assembly with the PG and/or cell division machinery. I will make use of chemicals that selectively target the cell cycle or cell division and monitor localization of S-layer assembly, will use nanobodies that disturb S-layer integrity and monitor the localization of cell wall synthesis, and use my interactomics experience to discover contact partners of S-layer and PG synthesis. Thus, SLYDIV is a multidisciplinary and integrative project that combines structural biology, biophysics, cell imaging, and microbiology. In addition, SLYDIV meets my solid knowledge on bacterial cell division with the host labs’ expertise on S-layer structure and function.
The SLYDIV project aims to lead to a major breakthrough in the basic understanding of the regulation of the bacterial cell envelope, while it will pave the way for specific novel molecular therapies against B. Anthracis, a Category A bioterrorist agent.
Unfold all
/
Fold all
More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/101062043 |
| Start date: | 01-09-2023 |
| End date: | 31-08-2025 |
| Total budget - Public funding: | - 175 920,00 Euro |
Cordis data
Original description
Many bacteria possess a paracrystaline protein coat named the S-layer. S-layers cover the entire cell surface and are involved in protection, virulence, cell-shape maintenance and communication. Lattice integrity is essential for S-layer function, meaning that its assembly must be intimately coordinated with cell growth and division. Some studies have reported that S-layer biogenesis co-localizes with peptidoglycan (PG) synthesis, however, the underlying molecular mechanisms remain unknown. Here, I will investigate the molecular regulatory network that orchestrates S-layer assembly, cell division and PG synthesis in the human pathogen Bacillus anthracis, where S-layer defects render the bacterium avirulent, making this ultrastructure an attractive therapeutic target.In the SLYDIV project I will 1) structurally and functionally compare Sap and EA1, the exponential and stationary phase S-layer proteins of B. anthracis 2) follow their in vivo assembly using time-resolved labelling and fluorescent microscopy and 3) uncovering the molecular interactions that couple S-layer assembly with the PG and/or cell division machinery. I will make use of chemicals that selectively target the cell cycle or cell division and monitor localization of S-layer assembly, will use nanobodies that disturb S-layer integrity and monitor the localization of cell wall synthesis, and use my interactomics experience to discover contact partners of S-layer and PG synthesis. Thus, SLYDIV is a multidisciplinary and integrative project that combines structural biology, biophysics, cell imaging, and microbiology. In addition, SLYDIV meets my solid knowledge on bacterial cell division with the host labs’ expertise on S-layer structure and function.
The SLYDIV project aims to lead to a major breakthrough in the basic understanding of the regulation of the bacterial cell envelope, while it will pave the way for specific novel molecular therapies against B. Anthracis, a Category A bioterrorist agent.
Status
SIGNEDCall topic
HORIZON-MSCA-2021-PF-01-01Update Date
09-02-2023
Images
No images available.
Geographical location(s)
