ExTzBox: A Glowing Cyclophane for Live-Cell Imaging

Indranil Roy, Sharan Bobbala, Jiawang Zhou, Minh T. Nguyen, Siva Krishna Mohan Nalluri, Yilei Wu, Daniel P. Ferris, Evan Alexander Scott, Michael R. Wasielewski, J. Fraser Stoddart*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

86 Scopus citations

Abstract

The ideal fluorescent probe for live-cell imaging is bright and non-cytotoxic and can be delivered easily into the living cells in an efficient manner. The design of synthetic fluorophores having all three of these properties, however, has proved to be challenging. Here, we introduce a simple, yet effective, strategy based on well-established chemistry for designing a new class of fluorescent probes for live-cell imaging. A box-like hybrid cyclophane, namely ExTzBox·4X (6·4X, X = PF6-, Cl-), has been synthesized by connecting an extended viologen (ExBIPY) and a dipyridyl thiazolothiazole (TzBIPY) unit in an end-to-end fashion with two p-xylylene linkers. Photophysical studies show that 6·4Cl has a quantum yield φF = 1.00. Furthermore, unlike its ExBIPY2+ and TzBIPY2+ building units, 6·4Cl is non-cytotoxic to RAW 264.7 macrophages, even with a loading concentration as high as 100 μM, presumably on account of its rigid box-like structure which prevents its intercalation into DNA and may inhibit other interactions with it. After gaining an understanding of the toxicity profile of 6·4Cl, we employed it in live-cell imaging. Confocal microscopy has demonstrated that 64+ is taken up by the RAW 264.7 macrophages, allowing the cells to glow brightly with blue laser excitation, without any hint of photobleaching or disruption of normal cell behavior under the imaging conditions. By contrast, the acyclic reference compound Me2TzBIPY·2Cl (4·2Cl) shows very little fluorescence inside the cells, which is quenched completely under the same imaging conditions. In vitro cell investigations underscore the significance of using highly fluorescent box-like rigid cyclophanes for live-cell imaging.

Original languageEnglish (US)
Pages (from-to)7206-7212
Number of pages7
JournalJournal of the American Chemical Society
Volume140
Issue number23
DOIs
StatePublished - Jun 13 2018

Funding

This research is part of the Joint Center of Excellence in Integrated Nano-Systems (JCIN) at King Abdulaziz City for Science and Technology (KACST) and Northwestern University (NU). The authors would like to thank both KACST and NU for their continued support of this research. This work was also supported by the Chemical Sciences Geosciences, and Biosciences Division, Office of Basic Energy Sciences U.S. Department of Energy under grant no. DE-FG02-99ER14999 (M.R.W.). This work was funded partly by the National Institutes of Health Director's New Innovator Award no. 1DP2HL132390-01. Y.W. thanks the Fulbright Scholar Program for a Fellowship and the NU International Institute of Nanotechnology for a Ryan Fellowship.

ASJC Scopus subject areas

  • General Chemistry
  • Biochemistry
  • Catalysis
  • Colloid and Surface Chemistry

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