Pal stabilises the bacterial outer membrane during constriction by a mobilisation-and-capture mechanism
Szczepaniak, J.; Holmes, P.; Rajasekar, K.; Kaminska, R.; Samsudin, F.; Inns, P. G.; Rassam, P.; Khalid, S.; Murray, S. M.; Redfield, C.; Kleanthous, C.
10.1101/790931 bioRxivShow abstract
Coordination of outer membrane constriction with septation is critical to faithful division in Gram-negative bacteria and vital to the barrier function of the membrane. Recent studies suggest this coordination is through the active accumulation of the peptidoglycan-binding outer membrane lipoprotein Pal at division sites by the Tol system, but the mechanism is unknown. Here, we show that Pal accumulation at Escherichia coli division sites is a consequence of three key functions of the Tol system. First, Tol mobilises Pal molecules in dividing cells, which otherwise diffuse very slowly due to their binding of the cell wall. Second, Tol actively captures mobilised Pal molecules and deposits them at the division septum. Third, the active capture mechanism is analogous to that used by the inner membrane protein TonB to dislodge the plug domains of outer membrane TonB-dependent nutrient transporters. We conclude that outer membrane constriction is coordinated with cell division by active mobilisation-and-capture of Pal at division septa by the Tol system.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- Fluoride triggers lysis in Streptococcus mutans by inhibition of Clp protease complex leading to an unabated competence cascade 96%
- Supramolecular assembly of the E. coli LdcI upon acid stress 96%
- Structural modeling reveals the allosteric switch controlling the chitin utilization program of Vibrio cholerae 96%
Similar papers in this journal
- The high-energy transition state of a membrane transporter 96%
- Lipopolysaccharide lateral mobility in the Gram-negative bacterial outer membrane is confined and governed by interactions within the conserved Lipid A anchor 96%
- An asymmetric nautilus-like HflK/C assembly controls FtsH proteolysis of membrane proteins 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.