Resistance to available antibiotics
poses a growing challenge
to
modern medicine, as this often disallows infections to be controlled.
This problem can only be alleviated by the development of new drugs.
Nisin, a natural lantibiotic with broad antimicrobial activity, has
shown promise as a potential candidate for combating antibiotic-resistant
bacteria. However, nisin is poorly soluble and barely stable at physiological
pH, which despite attempts to address these issues through mutant
design has restricted its use as an antibacterial drug. Therefore,
gaining a deeper understanding of the antimicrobial effectiveness,
which relies in part on its ability to form pores, is crucial for
finding innovative ways to manage infections caused by resistant bacteria.
Using large-scale molecular dynamics simulations, we find that the
bacterial membrane-specific lipid II increases the stability of pores
formed by nisin and that the interplay of nisin and lipid II reduces
the overall integrity of bacterial membranes by changing the local
thickness and viscosity