Researchers discovered a new tactic that bacteria use to fight to access nutrients. The discovery may allow for the development of new antibacterial agents in the future. The study results appeared in the scientific journal Science Advances, which also promoted the research on the cover. The work was co-financed by the Foundation for Polish Science within the TEAM* program, implemented from the Smart Growth Operational Programme (POIR).
Bacterial species are under continuous warfare with each other for access to nutrients. To gain an advantage in this struggle, they produce antibacterial compounds that target and kill their competitors. Different species of bacteria, including ones that live inside us, can battle each other for scarce resources using a variety of tactics. Now, researchers from the laboratories of Prof Jonathan Heddle from Malopolska Centre of Biotechnology, Jagiellonian University, Krakow and Dr Konstantinos Beis at Research Complex at Harwell, Imperial College, London, have uncovered the mechanism of one such tactic in work that may eventually lead to the development of new antibacterials.
The team’s work focussed on a protein called SbmA. In some bacteria this protein acts as an active gateway through the inner membrane of the cell, guarding the entrance to the cell interior. Bacteria use SbmA to “pump” much needed peptides into the cell where they can be used to make vital proteins. However, it can also be an Achilles heel: Other bacteria can ‘hijack’ SbmA by providing it with peptides that are toxic. When SbmA pumps in these poisons, the cell dies. The deviousness of this approach exploits the fact that SbmA seems able to pump in a wide variety of different peptides but exactly how it achieves this was unknown.
To gain more information into how SbmA works, the team, including lead authors Dmitry Ghilarov, Satomi Inaba-Inoue and Piotr Stępien, determined the structure of SbmA using cryo-electron microscopy at the Polish national cryo-EM facility (SOLARIS) and the UK’s national electron bio-imaging centre eBIC (Diamond Light Source).
The results, published in Science Advances, revealed a novel membrane protein fold, combining the features of ATP-powered and proton-powered transporters named SLiPT (“SbmA-like peptide transporters”).
Read the full paper in Science Advances: “Molecular mechanism of SbmA, a promiscuous transporter exploited by antimicrobial peptides,” available here: Link
Image shows A view of the determined SbmA structure in gold.
Image credit: ALINA KUROKHTINA
*The TEAM programme is implemented by the Foundation for Polish Science with EU funds from the European Regional Development Fund under the Smart Growth Operational Programme, Axis IV: Increasing the research potential, Measure 4.4 Increasing the human potential in the R&D sector.