Assessing Membrane Fluidity and Visualizing Fluid Membrane Domains in Bacteria Using Fluorescent Membrane Dyes
Journal article, 2018

Membrane fluidity is a key parameter of bacterial membranes that undergoes quick adaptation in response to environmental challenges and has recently emerged as an important factor in the antibacterial mechanism of membrane-targeting antibiotics. The specific level of membrane fluidity is not uniform across the bacterial cell membrane. Rather, specialized microdomains associated with different cellular functions can exhibit fluidity values that significantly deviate from the average. Assessing changes in the overall membrane fluidity and formation of membrane microdomains is therefore pivotal to understand both the functional organization of the bacterial cell membrane as well as antibiotic mechanisms. Here we describe how two fluorescent membrane dyes, laurdan and DiIC12, can be employed to assess membrane fluidity in living bacteria. We focus on Bacillus subtilis, since this organism has been relatively well-studied with respect to membrane domains. However, we also describe how these assays can be adapted for other bacteria such as Staphylococcus aureus and Streptococcus pneumoniae.

Laurdan GP

Cytoplasmic membrane

Antibiotic mode of action

RIFs

Membrane domains

Regions of increased fluidity.

Bacillus subtilis

Membrane fluidity

Author

Michaela Wenzel

University of Amsterdam

Norbert O. E. Vischer

University of Amsterdam

Henrik Strahl

Newcastle University

Leendert W. Hamoen

University of Amsterdam

Bio-protocol

23318325 (eISSN)

Vol. 8 20 e3063

Subject Categories (SSIF 2025)

Molecular Biology

Cell and Molecular Biology

Cell Biology

Microbiology

DOI

10.21769/BioProtoc.3063

More information

Latest update

3/23/2026