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Polymyxin B induces transient permeability fluctuations in asymmetric planar lipopolysaccharide/phospholipid bilayers
G Schröder1, K Brandenburg, U Seydel
1Division of Biophysics, Forschungsinstitut Borstel, Germany.
Abstract:
The interaction of the polycationic decapeptide polymyxin B with asymmetric planar bilayers from lipopolysaccharide and phospholipid monolayers, which resemble the lipid matrix of the outer membrane of Gram-negative bacteria, was investigated. The addition of polymyxin B in micromolar amounts to the lipopolysaccharide side of the asymmetric bilayers resulted, under voltage-clamp conditions, in a fast macroscopic increase of their ionic conductance, whereas the polymyxin B nonapeptide induced no significant conductance changes. The polymyxin B induced macroscopic conductance exhibited large fluctuations and was strongly dependent on the amplitude and polarity of the transmembrane potential. The temporal pattern and amplitudes of the fluctuations were characterized by power spectra of the membrane currents and their variances, respectively. In the initial phase following peptide addition, the conductance changes appeared to be channellike discrete fluctuations. The lifetimes of the fluctuations were exponentially distributed, and the mean lifetimes were strongly voltage-dependent, ranging from approximately 30 ms at +80 mV (positive at the side opposite to peptide addition) to less than 5 ms at reverse polarity. The conductance amplitudes of the single fluctuations exhibited a broad distribution with a mean of 2 nS. A comparison of the features of the macroscopic conductance and of the discrete fluctuations showed that the former can basically be understood as a superposition of a large number of the latter. From the amplitudes of the fluctuations, the diameter of the polymyxin-induced lesions was estimated to about 3 nm. The experimental findings can be understood by assuming a detergent-like action of polymyxin B.
Insights
Polymyxin B rapidly increases ionic conductance in bacterial outer membrane models by forming transient, voltage-dependent channels. These findings suggest a detergent-like mechanism for polymyxin B
Area of Science:
- Biophysics
- Membrane Biology
- Antimicrobial Peptides
Background:
- Gram-negative bacteria possess a unique outer membrane rich in lipopolysaccharide (LPS).
- Polymyxin B is a critical antibiotic targeting this outer membrane.
- Understanding polymyxin B's interaction mechanism is vital for combating bacterial infections.
Purpose of the Study:
- To investigate the interaction of polymyxin B with model lipid bilayers mimicking the Gram-negative outer membrane.
- To characterize the biophysical effects of polymyxin B on membrane conductance and structure.
Main Methods:
- Utilized asymmetric planar bilayers composed of LPS and phospholipids.
- Employed voltage-clamp techniques to measure ionic conductance changes.
- Analyzed membrane current fluctuations using power spectra and variances.
Main Results:
- Polymyxin B induced a rapid, voltage-dependent increase in ionic conductance.
- Observed channellike discrete fluctuations with voltage-dependent lifetimes.
- Estimated polymyxin B-induced lesion diameter to be approximately 3 nm.
Conclusions:
- Polymyxin B's action on bacterial membranes can be explained by a detergent-like mechanism.
- The observed conductance changes result from the superposition of numerous transient lesions.
- These findings provide insights into polymyxin B's antibacterial activity at the molecular level.