Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Visualization of nitric oxide in living cells by a copper-based fluorescent probe

Abstract

Nitric oxide (NO) serves as a messenger for cellular signaling. To visualize NO in living cells, we synthesized a turn-on fluorescent probe for use in combination with microscopy. Unlike existing fluorescent sensors, the construct—a Cu(II) complex of a fluorescein modified with an appended metal-chelating ligand (FL)—directly and immediately images NO rather than a derivative reactive nitrogen species. Using spectroscopic and mass spectrometric methods, we established that the mechanism of the reaction responsible for the NO-induced fluorescence involves reduction of the complex to Cu(I) with release of the nitrosated ligand, which occurs irreversibly. We detected NO produced by both constitutive and inducible NO synthases (cNOS and iNOS, respectively) in live neurons and macrophages in a concentration- and time-dependent manner by using the Cu(II)-based imaging agent. Both the sensitivity to nanomolar concentrations of NO and the spatiotemporal information provided by this complex demonstrate its value for numerous biological applications.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: The fluorescence response of CuFL to NO.
Figure 2: Specificity of CuFL for NO over other reactive nitrogen and oxygen species.
Figure 3: CuFL detection of NO produced by cNOS.
Figure 4: CuFL detection of NO produced by iNOS.
Figure 5: NO detection in SK-N-SH and Raw 264.7 cells by CuFL.

Similar content being viewed by others

References

  1. Murad, F. Discovery of some of the biological effects of nitric oxide and its role in cell signaling. Angew. Chem. Int. Edn. Engl. 38, 1856–1868 (1999).

    Article  CAS  Google Scholar 

  2. Furchgott, R.F. Endothelium-derived relaxing factor: discovery, early studies and identification as nitric oxide. Angew. Chem. Int. Edn. Engl. 38, 1870–1880 (1999).

    Article  CAS  Google Scholar 

  3. Ignarro, L.J. Nitric oxide a unique endogenous signaling molecule in vascular biology. Angew. Chem. Int. Edn. Engl. 38, 1882–1892 (1999).

    Article  CAS  Google Scholar 

  4. Packer, L. Methods in Enzymology, Nitric Oxide Part B, Physiological and Pathological Processes (Academic, San Diego, 1996).

    Google Scholar 

  5. Moncada, S., Palmer, R.M.J. & Higgs, E.A. Nitric oxide: physiology, pathphysiology, and pharmacology. Pharmacol. Rev. 43, 109–142 (1991).

    CAS  PubMed  Google Scholar 

  6. Ricciardolo, F.L.M., Sterk, P.J., Gaston, B. & Folkerts, G. Nitric oxide in health and disease of the respiratory system. Physiol. Rev. 84, 731–765 (2004).

    Article  CAS  PubMed  Google Scholar 

  7. Conner, E.M. & Grisham, M.B. Nitric oxide: biochemistry, physiology, and pathophysiology. Methods Enzymol. 7, 3–13 (1995).

    Article  CAS  Google Scholar 

  8. Hampl, V., Walters, C.L. & Archer, S.L. in Methods in Nitric Oxide Research (eds Feelisch, M. & Stamler, J.S.) 309–318 (John Wiley & Sons, New York, 1996).

    Google Scholar 

  9. Nagano, T. & Yoshimura, T. Bioimaging of nitric oxide. Chem. Rev. 102, 1235–1269 (2002).

    Article  CAS  PubMed  Google Scholar 

  10. Malinski, T., Mesaros, S. & Tomboulian, P. Nitric oxide measurement using electrochemical methods. Methods Enzymol. 268, 58–69 (1996).

    Article  CAS  PubMed  Google Scholar 

  11. Hilderbrand, S.A., Lim, M.H. & Lippard, S.J. in Topics in Fluorescence Spectroscopy (eds. Geddes, C.D. & Lakowicz, J.R.) 163–188 (Springer, Berlin, 2005).

    Book  Google Scholar 

  12. Sato, M., Hida, N. & Umezawa, Y. Imaging the nanomolar range of nitric oxide with an amplifier-coupled fluorescent indicator in living cells. Proc. Natl. Acad. Sci. USA 102, 14515–14520 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Miles, A.M., Chen, Y., Owens, M.W. & Grisham, M.B. Fluorometric determination of nitric oxide. Methods Enzymol. 7, 40–47 (1995).

    Article  CAS  Google Scholar 

  14. Sasaki, E. et al. Highly sensitive near-infrared fluorescent probes for nitric oxide and their application to isolated organs. J. Am. Chem. Soc. 127, 3684–3685 (2005).

    Article  CAS  PubMed  Google Scholar 

  15. Wink, D.A., Grisham, M.B., Mitchell, J.B. & Ford, P.C. Direct and indirect effects of nitric oxide in chemical reactions relevant to biology. Methods Enzymol. 268, 12–31 (1996).

    Article  CAS  PubMed  Google Scholar 

  16. Lozinsky, E.M. et al. Detection of nitric oxide from pig trachea by a fluorescence method. Anal. Biochem. 326, 139–145 (2004).

    Article  CAS  PubMed  Google Scholar 

  17. Nolan, E.M., Burdette, S.C., Harvey, J.H., Hilderbrand, S.A. & Lippard, S.J. Synthesis and characterization of zinc sensors based on a monosubstituted fluorescein platform. Inorg. Chem. 43, 2624–2635 (2004).

    Article  CAS  PubMed  Google Scholar 

  18. Sjöback, R., Nygren, J. & Kubista, M. Absorption and fluorescence properties of fluorescein. Spectrochim. Acta A Mol. Biomol. Spectrosc. 51, L7–L21 (1995).

    Article  Google Scholar 

  19. Bonnett, R., Holleyhead, R., Johnson, B.L. & Randall, E.W. Reaction of acidified nitrite solutions with peptide derivatives: Evidence for nitrosamine and thionitrite formation from 15N n. m. r. studies. J. Chem. Soc. Perkin I 22, 2261–2264 (1975).

    Article  Google Scholar 

  20. Karaghiosoff, K. et al. N-Nitroso- and N-nitraminotetrazoles. J. Org. Chem. 71, 1295–1305 (2006).

    Article  CAS  PubMed  Google Scholar 

  21. Lee, J., Chen, L., West, A.H. & Richter-Addo, G.B. Interactions of organic nitroso compunds with metals. Chem. Rev. 102, 1019–1066 (2002).

    Article  CAS  PubMed  Google Scholar 

  22. Tsuge, K., DeRosa, F., Lim, M.D. & Ford, P.C. Intramolecular reductive nitrosylation: reaction of nitric oxide and a copper(II) complex of a cyclam derivative with pendant luminescent chromophores. J. Am. Chem. Soc. 126, 6564–6565 (2004).

    Article  CAS  PubMed  Google Scholar 

  23. Lim, M.H. & Lippard, S.J. Copper complexes for fluorescence-based NO detection in aqueous solution. J. Am. Chem. Soc. 127, 12170–12171 (2005).

    Article  CAS  PubMed  Google Scholar 

  24. Smith, R.C., Tennyson, A.G., Lim, M.H. & Lippard, S.J. Conjugated polymer-based fluorescence turn-on sensor for nitric oxide. Org. Lett. 7, 3573–3575 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Xia, Y. & Krukoff, T.L. Estrogen induces nitric oxide production via activation of constitutive nitric oxide synthases in human neuroblastoma cells. Endocrinology 145, 4550–4557 (2004).

    Article  CAS  PubMed  Google Scholar 

  26. Marletta, M.A., Hurshman, A.R. & Rusche, K.M. Catalysis of nitric oxide synthase. Curr. Opin. Chem. Biol. 2, 656–663 (1998).

    Article  CAS  PubMed  Google Scholar 

  27. Wang, D. & Lippard, S.J. Cisplatin-induced post-translational modification of histones H3 and H4. J. Biol. Chem. 279, 20622–20625 (2004).

    Article  CAS  PubMed  Google Scholar 

  28. Miwa, M., Stuehr, D.J., Marletta, M.A., Wishnok, J.S. & Tannenbaum, S.R. Nitrosation of amines by stimulated macrophages. Carcinogenesis 8, 955–958 (1987).

    Article  CAS  PubMed  Google Scholar 

  29. Ralt, D., Wishnok, J.S., Fitts, R. & Tannenbaum, S.R. Bacterial catalysis of nitrosation: involvement of the nar Operon of Escherichia coli. J. Bacteriol. 170, 359–364 (1988).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Ji, X.-B. & Hollocher, T.C. Mechanism for nitrosation of 2,3-diaminonaphthalene by Escherichia coli: Enzymatic production of NO followed by O2-dependent chemical nitrosation. Appl. Environ. Microbiol. 54, 1791–1794 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Nakatsubo, N. et al. Direct evidence of nitric oxide production from bovine aortic endothelial cells using new fluorescence indicators: diaminofluoresceins. FEBS Lett. 427, 263–266 (1998).

    Article  CAS  PubMed  Google Scholar 

  32. Lijinsky, W. Chemistry and Biology of N-nitroso Compounds (eds. Coombs M.M., Ashby, J. & Hicks, M.) (Cambridge University Press, Cambridge, UK, 1992).

    Google Scholar 

  33. Koppenol, W.H. Thermodynamics of reactions involving nitrogen-oxygen compounds. Methods Enzymol. 268, 7–12 (1996).

    Article  CAS  PubMed  Google Scholar 

  34. Ford, P.C. & Lorkovic, I.M. Mechanistic aspects of the reactions of nitric oxide with transition-metal complexes. Chem. Rev. 102, 993–1017 (2002).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by grant CHE-0234951 from the US National Science Foundation (NSF). Spectroscopic instrumentation at the Massachusetts Institute of Technology Department of Chemistry Instrumentation Facility is maintained with funding from US National Institutes of Health Grant 1S10RR13886-01 and NSF Grants CHE-9808063, DBI9729592 and CHE-9808061. M.H. Lim thanks the Martin Family Society at the Massachusetts Institute of Technology for partial fellowship support. We thank A.Y. Ting and C.-W. Lin for assistance with epifluorescence microscopy, D.G. Nocera, D. Song and E.M. Nolan for helpful discussions, and C.D. Novina and D.M. Dykxhoorn for a gift of plasmid pcDNA3.1-Zeo(–)-U6 used in the RNAi experiments.

Author information

Authors and Affiliations

Authors

Contributions

M.H.L. and S.J.L. initiated, designed and performed the project. The RNAi experiment was carried out by D.X.

Corresponding author

Correspondence to Stephen J Lippard.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lim, M., Xu, D. & Lippard, S. Visualization of nitric oxide in living cells by a copper-based fluorescent probe. Nat Chem Biol 2, 375–380 (2006). https://doi.org/10.1038/nchembio794

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nchembio794

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing