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NBD derived diphenyl(aminomethyl)phosphane – A new fluorescent dye for imaging of low pH regions and lipid membranes in living cells

This work presents the comparative characterization (X-ray crystallography, NMR, solvatochromism and pH dependence of electronic absorption, steady-state and time resolved fluorescence properties) of a novel NBD based phosphane: 7-nitro-4-(4-(diphenylphosphinomethyl-piperazin-1-yl)-2,1,3-benzoxadiaz...

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Published in:Dyes and pigments 2021-01, Vol.184, p.108771, Article 108771
Main Authors: de Almeida, Rodrigo F.M., Santos, Tânia C.B., da Silva, Liana C., Suchodolski, Jakub, Krasowska, Anna, Stokowa-Sołtys, Kamila, Puchalska, Małgorzata, Starosta, Radosław
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container_end_page
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container_title Dyes and pigments
container_volume 184
creator de Almeida, Rodrigo F.M.
Santos, Tânia C.B.
da Silva, Liana C.
Suchodolski, Jakub
Krasowska, Anna
Stokowa-Sołtys, Kamila
Puchalska, Małgorzata
Starosta, Radosław
description This work presents the comparative characterization (X-ray crystallography, NMR, solvatochromism and pH dependence of electronic absorption, steady-state and time resolved fluorescence properties) of a novel NBD based phosphane: 7-nitro-4-(4-(diphenylphosphinomethyl-piperazin-1-yl)-2,1,3-benzoxadiazole (1) and an analogous compound: 7-nitro-4-(4-methyl-piperazin-1-yl)-2,1,3-benzoxadiazole (2). Protonated forms of the compounds are highly luminescent, while the neutral ones are not. The pKa values in water solutions are in the range 6.8–7.0 for 1 and 6.4–6.6 for 2. However, we showed that these values do not reflect the luminescence properties in more complex environments, where other equilibria may occur. Performance of 1 and 2 as potential molecular probes for biological imaging of living cells was evaluated towards mammalian (HEK 293T) and fungal cells (two Candida albicans strains: CAF2-1 - parental strain, and DSY1050 - mutant with no functional CDR1, CDR2 or MDR1 genes). For the HEK 293T cells, both compounds showed an intracellular punctuated bright staining typical of acidic compartments (late endosomes/lysosomes), as confirmed by co-localization with LysoView 633. In C. albicans the fungal cells, 1 labeled both organelle and plasma membranes, with similar behavior in both strains. For 2 the results indicated a different intracellular localization and an export of 2 by the cells through MDR transporters. In conclusion, our studies show that 1 and 2 can be the efficient cellular stains. Moreover, we expect that 1 can be also successfully used as a transition metal complexes fluorescent label, being a substitute for PPh3 or related phosphane ligands. [Display omitted] •CH3pip-NBD and Ph2PCH2-pip-NBD, a new fluorescent phosphane ligand, were synthesized.•X-ray structures, NMR, electronic absorption, and fluorescence characterization were discussed.•Both compounds proved to be efficient fluorescent cellular stains.•Compounds co-localize with LysoView 633 lysosomal tracker in mammalian HEK293T cells.•In Candida albicans cells, different localizations and behaviors were observed.
doi_str_mv 10.1016/j.dyepig.2020.108771
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Protonated forms of the compounds are highly luminescent, while the neutral ones are not. The pKa values in water solutions are in the range 6.8–7.0 for 1 and 6.4–6.6 for 2. However, we showed that these values do not reflect the luminescence properties in more complex environments, where other equilibria may occur. Performance of 1 and 2 as potential molecular probes for biological imaging of living cells was evaluated towards mammalian (HEK 293T) and fungal cells (two Candida albicans strains: CAF2-1 - parental strain, and DSY1050 - mutant with no functional CDR1, CDR2 or MDR1 genes). For the HEK 293T cells, both compounds showed an intracellular punctuated bright staining typical of acidic compartments (late endosomes/lysosomes), as confirmed by co-localization with LysoView 633. In C. albicans the fungal cells, 1 labeled both organelle and plasma membranes, with similar behavior in both strains. 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Protonated forms of the compounds are highly luminescent, while the neutral ones are not. The pKa values in water solutions are in the range 6.8–7.0 for 1 and 6.4–6.6 for 2. However, we showed that these values do not reflect the luminescence properties in more complex environments, where other equilibria may occur. Performance of 1 and 2 as potential molecular probes for biological imaging of living cells was evaluated towards mammalian (HEK 293T) and fungal cells (two Candida albicans strains: CAF2-1 - parental strain, and DSY1050 - mutant with no functional CDR1, CDR2 or MDR1 genes). For the HEK 293T cells, both compounds showed an intracellular punctuated bright staining typical of acidic compartments (late endosomes/lysosomes), as confirmed by co-localization with LysoView 633. In C. albicans the fungal cells, 1 labeled both organelle and plasma membranes, with similar behavior in both strains. For 2 the results indicated a different intracellular localization and an export of 2 by the cells through MDR transporters. In conclusion, our studies show that 1 and 2 can be the efficient cellular stains. Moreover, we expect that 1 can be also successfully used as a transition metal complexes fluorescent label, being a substitute for PPh3 or related phosphane ligands. 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Protonated forms of the compounds are highly luminescent, while the neutral ones are not. The pKa values in water solutions are in the range 6.8–7.0 for 1 and 6.4–6.6 for 2. However, we showed that these values do not reflect the luminescence properties in more complex environments, where other equilibria may occur. Performance of 1 and 2 as potential molecular probes for biological imaging of living cells was evaluated towards mammalian (HEK 293T) and fungal cells (two Candida albicans strains: CAF2-1 - parental strain, and DSY1050 - mutant with no functional CDR1, CDR2 or MDR1 genes). For the HEK 293T cells, both compounds showed an intracellular punctuated bright staining typical of acidic compartments (late endosomes/lysosomes), as confirmed by co-localization with LysoView 633. In C. albicans the fungal cells, 1 labeled both organelle and plasma membranes, with similar behavior in both strains. For 2 the results indicated a different intracellular localization and an export of 2 by the cells through MDR transporters. In conclusion, our studies show that 1 and 2 can be the efficient cellular stains. Moreover, we expect that 1 can be also successfully used as a transition metal complexes fluorescent label, being a substitute for PPh3 or related phosphane ligands. [Display omitted] •CH3pip-NBD and Ph2PCH2-pip-NBD, a new fluorescent phosphane ligand, were synthesized.•X-ray structures, NMR, electronic absorption, and fluorescence characterization were discussed.•Both compounds proved to be efficient fluorescent cellular stains.•Compounds co-localize with LysoView 633 lysosomal tracker in mammalian HEK293T cells.•In Candida albicans cells, different localizations and behaviors were observed.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.dyepig.2020.108771</doi><orcidid>https://orcid.org/0000-0001-6557-541X</orcidid><orcidid>https://orcid.org/0000-0002-9748-7083</orcidid><orcidid>https://orcid.org/0000-0002-3442-638X</orcidid></addata></record>
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subjects Candida albicans
Fluorescence imaging
Fluorescent label
HEK 293T
NBD fluorophore
Phosphine
title NBD derived diphenyl(aminomethyl)phosphane – A new fluorescent dye for imaging of low pH regions and lipid membranes in living cells
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