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Imaging Giant Vesicle Membrane Domains with a Luminescent Europium Tetracycline Complex
[Image: see text] 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 wi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433515/ https://www.ncbi.nlm.nih.gov/pubmed/37599986 http://dx.doi.org/10.1021/acsomega.3c02721 |
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author | Cawley, Jennie L. Berger, Brett A. Odudimu, Adeyemi T. Singh, Aarshi N. Santa, Dane E. McDarby, Ariana I. Honerkamp-Smith, Aurelia R. Wittenberg, Nathan J. |
author_facet | Cawley, Jennie L. Berger, Brett A. Odudimu, Adeyemi T. Singh, Aarshi N. Santa, Dane E. McDarby, Ariana I. Honerkamp-Smith, Aurelia R. Wittenberg, Nathan J. |
author_sort | Cawley, Jennie L. |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-10433515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104335152023-08-18 Imaging Giant Vesicle Membrane Domains with a Luminescent Europium Tetracycline Complex Cawley, Jennie L. Berger, Brett A. Odudimu, Adeyemi T. Singh, Aarshi N. Santa, Dane E. McDarby, Ariana I. Honerkamp-Smith, Aurelia R. Wittenberg, Nathan J. ACS Omega [Image: see text] 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. American Chemical Society 2023-08-01 /pmc/articles/PMC10433515/ /pubmed/37599986 http://dx.doi.org/10.1021/acsomega.3c02721 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/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/). |
spellingShingle | Cawley, Jennie L. Berger, Brett A. Odudimu, Adeyemi T. Singh, Aarshi N. Santa, Dane E. McDarby, Ariana I. Honerkamp-Smith, Aurelia R. Wittenberg, Nathan J. Imaging Giant Vesicle Membrane Domains with a Luminescent Europium Tetracycline Complex |
title | Imaging Giant Vesicle
Membrane Domains with a Luminescent
Europium Tetracycline Complex |
title_full | Imaging Giant Vesicle
Membrane Domains with a Luminescent
Europium Tetracycline Complex |
title_fullStr | Imaging Giant Vesicle
Membrane Domains with a Luminescent
Europium Tetracycline Complex |
title_full_unstemmed | Imaging Giant Vesicle
Membrane Domains with a Luminescent
Europium Tetracycline Complex |
title_short | Imaging Giant Vesicle
Membrane Domains with a Luminescent
Europium Tetracycline Complex |
title_sort | imaging giant vesicle
membrane domains with a luminescent
europium tetracycline complex |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433515/ https://www.ncbi.nlm.nih.gov/pubmed/37599986 http://dx.doi.org/10.1021/acsomega.3c02721 |
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