Issue 10, 2023

Polar ammoniostyryls easily converting a clickable lipophilic BODIPY in an advanced plasma membrane probe

Abstract

A very simple, small and symmetric, but highly bright, photostable and functionalizable molecular probe for plasma membrane (PM) has been developed from an accessible, lipophilic and clickable organic dye based on BODIPY. To this aim, two lateral polar ammoniostyryl groups were easily linked to increase the amphiphilicity of the probe and thus its lipid membrane partitioning. Compared to the BODIPY precursor, the transversal diffusion across lipid bilayers of the ammoniostyryled BODIPY probe was highly reduced, as evidenced by fluorescence confocal microscopy on model membranes built up as giant unilamellar vesicles (GUVs). Moreover, the ammoniostyryl groups endow the new BODIPY probe with the ability to optically work (excitation and emission) in the bioimaging-useful red region, as shown by staining of the plasma membrane of living mouse embryonic fibroblasts (MEFs). Upon incubation, this fluorescent probe rapidly entered the cell through the endosomal pathway. By blocking the endocytic trafficking at 4 °C, the probe was confined within the PM of MEFs. Our experiments show the developed ammoniostyrylated BODIPY as a suitable PM fluorescent probe, and confirm the synthetic approach for advancing PM probes, imaging and science.

Graphical abstract: Polar ammoniostyryls easily converting a clickable lipophilic BODIPY in an advanced plasma membrane probe

  • This article is part of the themed collection: #MyFirstJMCB

Supplementary files

Article information

Article type
Paper
Submitted
17 Nov 2022
Accepted
12 Feb 2023
First published
13 Feb 2023

J. Mater. Chem. B, 2023,11, 2108-2114

Polar ammoniostyryls easily converting a clickable lipophilic BODIPY in an advanced plasma membrane probe

S. Serrano-Buitrago, M. Muñoz-Úbeda, V. G. Almendro-Vedia, J. Sánchez-Camacho, B. L. Maroto, F. Moreno, J. Bañuelos, I. García-Moreno, I. López-Montero and S. de la Moya, J. Mater. Chem. B, 2023, 11, 2108 DOI: 10.1039/D2TB02516G

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