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      Imaging Giant Vesicle Membrane Domains with a Luminescent Europium Tetracycline Complex

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          Abstract

          Microdomains in lipid bilayer membranes are routinely imaged using organic fluorophores that preferentially partition into one of the lipid phases, resulting in fluorescence contrast. Here, we show that membrane microdomains in giant unilamellar vesicles (GUVs) can be visualized with europium luminescence using a complex of europium III (Eu 3+) and tetracycline (EuTc). EuTc is unlike typical organic lipid probes in that it is a coordination complex with a unique excitation/emission wavelength combination (396/617 nm), a very large Stokes shift (221 nm), and a very narrow emission bandwidth (8 nm). The probe preferentially interacts with liquid disordered domains in GUVs, which results in intensity contrast across the surface of phase-separated GUVs. Interestingly, EuTc also alters GM1 ganglioside partitioning. GM1 typically partitions into liquid ordered domains, but after labeling phase-separated GUVs with EuTc, cholera toxin B-subunit (CTxB), which binds GM1, labels liquid disordered domains. We also demonstrate that EuTc, but not free Eu 3+ or Tc, significantly reduces lipid diffusion coefficients. Finally, we show that EuTc can be used to label cellular membranes similar to a traditional membrane probe. EuTc may find utility as a membrane imaging probe where its large Stokes shift and sharp emission band would enable multicolor imaging.

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          Lipid rafts as a membrane-organizing principle.

          Cell membranes display a tremendous complexity of lipids and proteins designed to perform the functions cells require. To coordinate these functions, the membrane is able to laterally segregate its constituents. This capability is based on dynamic liquid-liquid immiscibility and underlies the raft concept of membrane subcompartmentalization. Lipid rafts are fluctuating nanoscale assemblies of sphingolipid, cholesterol, and proteins that can be stabilized to coalesce, forming platforms that function in membrane signaling and trafficking. Here we review the evidence for how this principle combines the potential for sphingolipid-cholesterol self-assembly with protein specificity to selectively focus membrane bioactivity.
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            Interpretation of europium(III) spectra

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              Liposomes and polymersomes: a comparative review towards cell mimicking

              Minimal cells: we compare and contrast liposomes and polymersomes for a better a priori choice and design of vesicles and try to understand the advantages and shortcomings associated with using one or the other in many different aspects (properties, synthesis, self-assembly, applications). Cells are integral to all forms of life due to their compartmentalization by the plasma membrane. However, living organisms are immensely complex. Thus there is a need for simplified and controllable models of life for a deeper understanding of fundamental biological processes and man-made applications. This is where the bottom-up approach of synthetic biology comes from: a stepwise assembly of biomimetic functionalities ultimately into a protocell. A fundamental feature of such an endeavor is the generation and control of model membranes such as liposomes and polymersomes. We compare and contrast liposomes and polymersomes for a better a priori choice and design of vesicles and try to understand the advantages and shortcomings associated with using one or the other in many different aspects (properties, synthesis, self-assembly, applications) and which aspects have been studied and developed with each type and update the current development in the field.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                01 August 2023
                15 August 2023
                : 8
                : 32
                : 29314-29323
                Affiliations
                []Department of Chemistry, Lehigh University , 6 East Packer Avenue, Bethlehem, Pennsylvania 18015, United States
                []Department of Physics, Lehigh University , 17 Memorial Drive East, Bethlehem, Pennsylvania 18015, United States
                Author notes
                Author information
                https://orcid.org/0009-0001-6641-2003
                https://orcid.org/0000-0002-6506-481X
                https://orcid.org/0000-0002-5888-4449
                https://orcid.org/0000-0003-1337-0396
                https://orcid.org/0000-0001-8149-5735
                https://orcid.org/0000-0002-5986-4706
                https://orcid.org/0000-0001-9196-1867
                Article
                10.1021/acsomega.3c02721
                10433515
                5beded0f-4559-4199-af38-3a9b54178fe7
                © 2023 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 20 April 2023
                : 24 July 2023
                Funding
                Funded by: National Science Foundation, doi 10.13039/100000001;
                Award ID: 2044792
                Funded by: Lehigh University, doi 10.13039/100008234;
                Award ID: NA
                Categories
                Article
                Custom metadata
                ao3c02721
                ao3c02721

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