Mapping membrane biophysical nano-environments

The mammalian plasma membrane is known to contain domains with varying lipid composition and biophysical properties. However, studying these membrane lipid domains presents challenges due to their predicted morphological similarity to the bulk membrane and their scale being below the classical resolution limit of optical microscopy. To address this, we combine the solvatochromic probe di-4-ANEPPDHQ, which reports on its biophysical environment through changes in its fluorescence emission, with spectrally resolved single-molecule localisation microscopy. The resulting data comprises nanometre-precision localisation coordinates and a generalised polarisation value related to the probe's environment - a marked point pattern. We introduce quantification algorithms based on topological data analysis (PLASMA) to detect and map nano-domains in this marked data, demonstrating their effectiveness in both artificial membranes and live cells. By leveraging environmentally sensitive fluorophores, multi-modal single molecule localisation microscopy, and advanced analysis methods, we achieve nanometre scale mapping of membrane properties and assess changes in response to external perturbation with methyl-β-cyclodextrin. This integrated methodology represents an integrated toolset for investigating marked point pattern data at nanometre spatial scales.

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Publication Details

Journal
Nature Communications
Published
2024-11-07
DOI
https://doi.org/10.1038/s41467-024-53883-1
Citations
15
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
3.51

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article

Mapping membrane biophysical nano-environments

Maria Makarova, Dylan M. Owen, Jonas Euchner, Stanimir Asenov Tashev et al.
15 citations
Nature Communications
Lipid Membrane Structure and Behavior
3.51
article

Mapping membrane biophysical nano-environments

Maria Makarova, Dylan M. Owen, Jonas Euchner, Stanimir Asenov Tashev, Luca Panconi, Dirk‐Peter Herten, Daniel J. Nieves
article en
15 citations

Abstract

The mammalian plasma membrane is known to contain domains with varying lipid composition and biophysical properties. However, studying these membrane lipid domains presents challenges due to their predicted morphological similarity to the bulk membrane and their scale being below the classical resolution limit of optical microscopy. To address this, we combine the solvatochromic probe di-4-ANEPPDHQ, which reports on its biophysical environment through changes in its fluorescence emission, with spectrally resolved single-molecule localisation microscopy. The resulting data comprises nanometre-precision localisation coordinates and a generalised polarisation value related to the probe's environment - a marked point pattern. We introduce quantification algorithms based on topological data analysis (PLASMA) to detect and map nano-domains in this marked data, demonstrating their effectiveness in both artificial membranes and live cells. By leveraging environmentally sensitive fluorophores, multi-modal single molecule localisation microscopy, and advanced analysis methods, we achieve nanometre scale mapping of membrane properties and assess changes in response to external perturbation with methyl-β-cyclodextrin. This integrated methodology represents an integrated toolset for investigating marked point pattern data at nanometre spatial scales.

Nature CommunicationsVol. 15(1)
University College Birmingham (GB), NIHR Surgical Reconstruction and Microbiology Research Centre (GB), University of Birmingham (GB)
Academy of Medical Sciences, Engineering and Physical Sciences Research Council
Life in Land
Openalex Percentile: Top 6%
Lipid Membrane Structure and Behavior
3.51
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