4.5 Article

From LUVs to GUVs- How to Cover Micrometer-Sized Pores with Membranes

期刊

JOURNAL OF PHYSICAL CHEMISTRY B
卷 126, 期 41, 页码 8233-8244

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.2c05685

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资金

  1. Deutsche Forschungsgemeinschaft (DFG, Research Foundation Germany) under Germany's Excellence Strategy [EXC 2067-390729940, JA963/19-1, STE884/18-1]
  2. VW Foundation (Living Foams)

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Pore-spanning membranes (PSMs) are a versatile tool for investigating membrane-confined processes. Fluorescence microscopy is most suitable for visualizing PSMs with micrometer-sized pores. However, the current method for preparing PSMs relies on the spreading of giant unilamellar vesicles (GUVs), which has limitations. In this study, a new method using droplet-stabilized GUVs generated in a microfluidic device was developed to produce PSMs from large unilamellar vesicles. The diffusion and mechanical properties of the resulting PSMs were analyzed and compared to PSMs derived from electroformed GUVs, showing that the GUV formation procedure has little impact on lipid diffusion and mechanical properties.
Pore-spanning membranes (PSMs) are a versatile tool to investigate membrane-confined processes in a bottom-up approach. Pore sizes in the micrometer range are most suited to visualize PSMs using fluorescence microscopy. However, the preparation of these PSMs relies on the spreading of giant unilamellar vesicles (GUVs). GUV production faces several limitations. Thus, alternative ways to generate PSMs starting from large or small unilamellar vesicles that are more reproducibly prepared are highly desirable. Here we describe a method to produce PSMs obtained from large unilamellar vesicles, making use of droplet-stabilized GUVs generated in a microfluidic device. We analyzed the lipid diffusion in the free-standing and supported parts of the PSMs using z-scan fluorescence correlation spectroscopy and fluorescence recovery after photobleaching experiments in combination with finite element simulations. Employing atomic force indentation experiments, we also investigated the mechanical properties of the PSMs. Both lipid diffusion constants and lateral membrane tension were compared to those obtained on PSMs derived from electroformed GUVs, which are known to be solvent-and detergent-free, under otherwise identical conditions. Our results demonstrate that the lipid diffusion, as well as the mechanical properties of the resulting PSMs, is almost unaffected by the GUV formation procedure but depends on the chosen substrate functionalization. With the new method in hand, we were able to reconstitute the syntaxin-1A transmembrane domain in microfluidic GUVs and PSMs, which was visualized by fluorescence microscopy.

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