Assessing Membrane Fluidity and Visualizing Fluid Membrane Domains in Bacteria Using Fluorescent Membrane Dyes
Artikel i vetenskaplig tidskrift, 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

Författare

Michaela Wenzel

Universiteit Van Amsterdam

Norbert O. E. Vischer

Universiteit Van Amsterdam

Henrik Strahl

Newcastle University

Leendert W. Hamoen

Universiteit Van Amsterdam

Bio-protocol

23318325 (eISSN)

Vol. 8 20 e3063

Ämneskategorier (SSIF 2025)

Molekylärbiologi

Cell- och molekylärbiologi

Cellbiologi

Mikrobiologi

DOI

10.21769/BioProtoc.3063

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Senast uppdaterat

2026-03-23