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用发光的铕四环素配合物成像巨型囊泡膜结构域

Imaging Giant Vesicle Membrane Domains with a Luminescent Europium Tetracycline Complex.

作者信息

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

机构信息

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.

出版信息

ACS Omega. 2023 Aug 1;8(32):29314-29323. doi: 10.1021/acsomega.3c02721. eCollection 2023 Aug 15.

DOI:10.1021/acsomega.3c02721
PMID:37599986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10433515/
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) 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 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.

摘要

脂质双分子层膜中的微区通常使用优先分配到其中一个脂质相的有机荧光团进行成像,从而产生荧光对比度。在此,我们表明,使用铕(III)(Eu)与四环素(EuTc)的复合物,通过铕发光可以观察到巨型单层囊泡(GUVs)中的膜微区。EuTc不同于典型的有机脂质探针,它是一种配位复合物,具有独特的激发/发射波长组合(396/617 nm)、非常大的斯托克斯位移(221 nm)和非常窄的发射带宽(8 nm)。该探针优先与GUVs中的液相无序区相互作用,这导致相分离GUVs表面出现强度对比度。有趣的是,EuTc还会改变GM1神经节苷脂的分配。GM1通常分配到液相有序区,但在用EuTc标记相分离的GUVs后,与GM1结合的霍乱毒素B亚基(CTxB)标记液相无序区。我们还证明,EuTc而非游离的Eu或Tc会显著降低脂质扩散系数。最后,我们表明EuTc可用于标记细胞膜,类似于传统的膜探针。EuTc因其大的斯托克斯位移和尖锐的发射带可能作为膜成像探针发挥作用,从而实现多色成像。

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