A water-soluble, long fluorescent lifetime DNA probe for real-time dynamic visualization of mitosis in live cells and applicability for FLIM/time-gated imaging

Long-lived and photostable fluorescent probes for real-time monitoring of cell division, particularly for dynamic visualization of mitosis and interphase, are rare. We have developed a water-soluble diazaoxatriangulenium cation-based fluorescent probe, Nuc-DAOTA+, that meets these criteria. Nuc-DAOTA+ has a long fluorescence lifetime (∼20 ns) and exclusively targets the nucleus for specific DNA binding in live cells, essential for real-time dynamic imaging of cell-division, including mitosis and interphase. Addition of dsDNA (0-50 μg mL<sup>-1</sup>) to Nuc-DAOTA+ results in a red shift (∼10 nm) of the absorption and a blue shift (∼5 nm) of the fluorescence maxima, along with an intensity increase in both. A very good linear correlation (<i>R</i><sup>2</sup> = 0.999) from the plot of fluorescence intensity <i>versus</i> concentration of dsDNA (up to 30 μg mL<sup>-1</sup>) resulted in a detection limit of 0.7 μg mL<sup>-1</sup>. The Benesi-Hildebrand plot was used to calculate the binding constant between the Nuc-DAOTA+ and DNA, which was found to be 1.6 × 10<sup>4</sup> M<sup>-1</sup> and the mechanism of binding interactions was investigated using CD spectroscopy. The long fluorescence lifetime and excellent biocompatibility of Nuc-DAOTA+ enabled its use for real-time dynamic imaging of mitotic phases and interphase in live CHO (Chinese hamster ovary) cells by using confocal microscopy. In addition, the Nuc-DAOTA+ exhibited high photostability during photo-bleaching experiments and was successfully applied for fluorescence lifetime imaging microscopy (FLIM) and time gated imaging of the mouse embryonic fibroblast 3T3 cell line.

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Publication Details

Journal
Journal of Materials Chemistry B
Published
2025-01-01
DOI
https://doi.org/10.1039/d5tb00404g
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
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article

A water-soluble, long fluorescent lifetime DNA probe for real-time dynamic visualization of mitosis in live cells and applicability for FLIM/time-gated imaging

Bo W. Laursen, Thomas Hartig Braunstein, Pablo Hernández-Varas, Mikkel Baldtzer Liisberg et al.
2 links
Journal of Materials Chemistry B
DNA and Nucleic Acid Chemistry
article

A water-soluble, long fluorescent lifetime DNA probe for real-time dynamic visualization of mitosis in live cells and applicability for FLIM/time-gated imaging

Bo W. Laursen, Thomas Hartig Braunstein, Pablo Hernández-Varas, Mikkel Baldtzer Liisberg, Kapil Kumar
article en

Abstract

Long-lived and photostable fluorescent probes for real-time monitoring of cell division, particularly for dynamic visualization of mitosis and interphase, are rare. We have developed a water-soluble diazaoxatriangulenium cation-based fluorescent probe, Nuc-DAOTA+, that meets these criteria. Nuc-DAOTA+ has a long fluorescence lifetime (∼20 ns) and exclusively targets the nucleus for specific DNA binding in live cells, essential for real-time dynamic imaging of cell-division, including mitosis and interphase. Addition of dsDNA (0-50 μg mL<sup>-1</sup>) to Nuc-DAOTA+ results in a red shift (∼10 nm) of the absorption and a blue shift (∼5 nm) of the fluorescence maxima, along with an intensity increase in both. A very good linear correlation (<i>R</i><sup>2</sup> = 0.999) from the plot of fluorescence intensity <i>versus</i> concentration of dsDNA (up to 30 μg mL<sup>-1</sup>) resulted in a detection limit of 0.7 μg mL<sup>-1</sup>. The Benesi-Hildebrand plot was used to calculate the binding constant between the Nuc-DAOTA+ and DNA, which was found to be 1.6 × 10<sup>4</sup> M<sup>-1</sup> and the mechanism of binding interactions was investigated using CD spectroscopy. The long fluorescence lifetime and excellent biocompatibility of Nuc-DAOTA+ enabled its use for real-time dynamic imaging of mitotic phases and interphase in live CHO (Chinese hamster ovary) cells by using confocal microscopy. In addition, the Nuc-DAOTA+ exhibited high photostability during photo-bleaching experiments and was successfully applied for fluorescence lifetime imaging microscopy (FLIM) and time gated imaging of the mouse embryonic fibroblast 3T3 cell line.

Journal of Materials Chemistry BVol. 13(40)
Roskilde University (DK), University of Copenhagen (DK), VIB-KU Leuven Center for Brain & Disease Research (BE)
Openalex Percentile: Top 80%
DNA and Nucleic Acid Chemistry
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