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  Pore-spanning membranes as a tool to investigate lateral lipid membrane heterogeneity

Socrier, L., & Steinem, C. (2024). Pore-spanning membranes as a tool to investigate lateral lipid membrane heterogeneity. Methods in Enzymology, in press. doi:10.1016/bs.mie.2024.02.009.

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Socrier, Larissa1, Author           
Steinem, Claudia1, Author           
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1Max Planck Fellow Group Membrane-based biomimetic nano- and micro-compartments, Max Planck Institute for Dynamics and Self-Organization, Max Planck Society, ou_2586691              

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 Abstract: Over the years, it has become more and more obvious that lipid membranes show a very complex behavior. This behavior arises in part from the large number of different kinds of lipids and proteins and how they dynamically interact with each other. In vitro studies using artificial membrane systems have shed light on the heterogeneity based on lipid-lipid interactions in multicomponent bilayer mixtures. Inspired by the raft hypothesis, the coexistence of liquid-disordered (ld) and liquid-ordered (lo) phases has drawn much attention. It was shown that ternary lipid mixtures containing low- and high-melting temperature lipids and cholesterol can phase separate into a lo phase enriched in the high-melting lipids and cholesterol and a ld phase enriched in the low-melting lipids. Depending on the model membrane system under investigation, different domain sizes, shapes, and mobilities have been found.

Here, we describe how to generate phase-separated lo/ld phases in model membrane systems termed pore-spanning membranes (PSMs). These PSMs are prepared on porous silicon substrates with pore sizes in the micrometer regime. A proper functionalization of the top surface of the substrates is required to achieve the spreading of giant unilamellar vesicles (GUVs) to obtain PSMs. Starting with lo/ld phase-separated GUVs lead to membrane heterogeneities in the PSMs. Depending on the functionalization strategy of the top surface of the silicon substrate, different membrane heterogeneities are observed in the PSMs employing fluorescence microscopy. A quantitative analysis of the heterogeneity as well as the dynamics of the lipid domains is described.

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Language(s): eng - English
 Dates: 2024-03-05
 Publication Status: Published online
 Pages: -
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 Rev. Type: Peer
 Identifiers: DOI: 10.1016/bs.mie.2024.02.009
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Title: Methods in Enzymology
  Other : Methods Enzymol.
Source Genre: Journal
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Publ. Info: New York, NY : Academic Press
Pages: - Volume / Issue: - Sequence Number: in press Start / End Page: - Identifier: ISSN: 0076-6879
CoNE: https://pure.mpg.de/cone/journals/resource/110975506069301