Surface Chemistry of Cytosporone-B Incorporated in Models for Microbial Biomembranes as Langmuir Monolayers

TL;DR

This study explores how cytosporone-B affects microbial biomembrane models, showing different impacts on two types of lipid monolayers.

Contribution

The paper reveals how cytosporone-B alters membrane properties in fluid and condensed states without causing aggregation.

Findings

Cytosporone-B expanded DPPE monolayers and condensed DOPE monolayers.

The drug reduced compressibility modulus more significantly in DPPE.

Surface potential measurements showed increased acyl chain tilt in DOPE.

Abstract

Cytosporone-B, a polyketide renowned for its antimicrobial
properties,
was integrated into Langmuir monolayers composed of dipalmitoylphosphoethanolamine
(DPPE) and dioleoylphosphoethanolamine (DOPE) lipids, effectively
emulating microbial cytoplasmic membranes. This compound exhibited
an expansive influence on DPPE monolayers while inducing condensation
in DOPE monolayers. This led to a notable reduction in the compressibility
modulus for both lipids, with a more pronounced effect observed for
DPPE. The heightened destabilization observed in DOPE monolayers subjected
to biologically relevant pressures was particularly noteworthy, as
evidenced by surface pressure–time curves at constant area.
In-depth analysis using infrared spectroscopy at the air–water
interface unveiled alterations in the alkyl chains of the lipids induced
by cytosporone-B. This was further corroborated by surface potential
measurements, indicating a heightened tilt in the acyl chains upon
drug incorporation. Notably, these observed effects did not indicate
an aggregating process induced by the drug. Overall, the distinctive
impact of cytosporone-B on each lipid underscores the importance of
understanding the nuanced effects of microbial drugs on membranes,
whether in condensed or fluid states.

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