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.

  • Perspective
  • Published:

Immunolabeling artifacts and the need for live-cell imaging

Abstract

Fluorescent fusion proteins have revolutionized examination of proteins in living cells. Still, studies using these proteins are met with criticism because proteins are modified and ectopically expressed, in contrast to immunofluorescence studies. However, introducing immunoreagents inside cells can cause protein extraction or relocalization, not reflecting the in vivo situation. Here we discuss pitfalls of immunofluorescence labeling that often receive little attention and argue that immunostaining experiments in dead, permeabilized cells should be complemented with live-cell imaging when scrutinizing protein localization.

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: Fixation and permeabilization can affect epitope accessibility.
Figure 2: Effects of standard fixation and permeabilization protocols on protein localization and epitope accessibility in different cell lines.
Figure 3: Effects of standard immunostaining methods on protein extraction and EGFP fluorescence.
Figure 4: Ultrastructural changes after fixation and permeabilization.

Similar content being viewed by others

References

  1. Giepmans, B.N., Adams, S.R., Ellisman, M.H. & Tsien, R.Y. The fluorescent toolbox for assessing protein location and function. Science 312, 217–224 (2006).

    Article  CAS  Google Scholar 

  2. Schermelleh, L., Heintzmann, R. & Leonhardt, H. A guide to super-resolution fluorescence microscopy. J. Cell Biol. 190, 165–175 (2010).

    Article  CAS  Google Scholar 

  3. Humbel, B.M., de Jong, M.D., Muller, W.H. & Verkleij, A.J. Pre-embedding immunolabeling for electron microscopy: an evaluation of permeabilization methods and markers. Microsc. Res. Tech. 42, 43–58 (1998).

    Article  CAS  Google Scholar 

  4. Giepmans, B.N., Deerinck, T.J., Smarr, B.L., Jones, Y.Z. & Ellisman, M.H. Correlated light and electron microscopic imaging of multiple endogenous proteins using Quantum dots. Nat. Methods 2, 743–749 (2005).

    Article  CAS  Google Scholar 

  5. Shaner, N.C., Steinbach, P.A. & Tsien, R.Y. A guide to choosing fluorescent proteins. Nat. Methods 2, 905–909 (2005).

    Article  CAS  Google Scholar 

  6. Tsien, R.Y. The green fluorescent protein. Annu. Rev. Biochem. 67, 509–544 (1998).

    Article  CAS  Google Scholar 

  7. Chudakov, D.M., Matz, M.V., Lukyanov, S. & Lukyanov, K.A. Fluorescent proteins and their applications in imaging living cells and tissues. Physiol. Rev. 90, 1103–1163 (2010).

    Article  CAS  Google Scholar 

  8. Palmer, A.E., Qin, Y., Park, J.G. & McCombs, J.E. Design and application of genetically encoded biosensors. Trends Biotechnol. 29, 144–152 (2011).

    Article  CAS  Google Scholar 

  9. Piehl, M. & Cassimeris, L. Organization and dynamics of growing microtubule plus ends during early mitosis. Mol. Biol. Cell 14, 916–925 (2003).

    Article  CAS  Google Scholar 

  10. Melan, M.A. Overview of cell fixatives and cell membrane permeants. Methods Mol. Biol. 115, 45–55 (1999).

    CAS  PubMed  Google Scholar 

  11. Howell, B., Deacon, H. & Cassimeris, L. Decreasing oncoprotein 18/stathmin levels reduces microtubule catastrophes and increases microtubule polymer in vivo. J. Cell Sci. 112, 3713–3722 (1999).

    CAS  PubMed  Google Scholar 

  12. Hoetelmans, R.W. et al. Effects of acetone, methanol, or paraformaldehyde on cellular structure, visualized by reflection contrast microscopy and transmission and scanning electron microscopy. Appl. Immunohistochem. Mol. Morphol. 9, 346–351 (2001).

    CAS  PubMed  Google Scholar 

  13. Stadler, C., Skogs, M., Brismar, H., Uhlen, M. & Lundberg, E. A single fixation protocol for proteome-wide immunofluorescence localization studies. J. Proteomics 73, 1067–1078 (2010).

    Article  CAS  Google Scholar 

  14. Wang, D.S., Miller, R., Shaw, R. & Shaw, G. The pleckstrin homology domain of human beta I sigma II spectrin is targeted to the plasma membrane in vivo. Biochem. Biophys. Res. Commun. 225, 420–426 (1996).

    Article  CAS  Google Scholar 

  15. Jamur, M.C. & Oliver, C. Cell fixatives for immunostaining. Methods Mol. Biol. 588, 55–61 (2010).

    Article  Google Scholar 

  16. Jamur, M.C. & Oliver, C. Permeabilization of cell membranes. Methods Mol. Biol. 588, 63–66 (2010).

    Article  Google Scholar 

  17. Hannah, M.J., Weiss, U. & Huttner, W.B. Differential extraction of proteins from paraformaldehyde-fixed cells: lessons from synaptophysin and other membrane proteins. Methods 16, 170–181 (1998).

    Article  CAS  Google Scholar 

  18. Goldenthal, K.L., Hedman, K., Chen, J.W., August, J.T. & Willingham, M.C. Postfixation detergent treatment for immunofluorescence suppresses localization of some integral membrane proteins. J. Histochem. Cytochem. 33, 813–820 (1985).

    Article  CAS  Google Scholar 

  19. Neuhaus, E.M., Horstmann, H., Almers, W., Maniak, M. & Soldati, T. Ethane-freezing/methanol-fixation of cell monolayers: a procedure for improved preservation of structure and antigenicity for light and electron microscopies. J. Struct. Biol. 121, 326–342 (1998).

    Article  CAS  Google Scholar 

  20. Schimenti, K.J. & Jacobberger, J.W. Fixation of mammalian cells for flow cytometric evaluation of DNA content and nuclear immunofluorescence. Cytometry 13, 48–59 (1992).

    Article  CAS  Google Scholar 

  21. Hoetelmans, R.W., van Slooten, H.J., Keijzer, R., van de Velde, C.J. & van Dierendonck, J.H. Routine formaldehyde fixation irreversibly reduces immunoreactivity of Bcl-2 in the nuclear compartment of breast cancer cells, but not in the cytoplasm. Appl. Immunohistochem. Mol. Morphol. 9, 74–80 (2001).

    CAS  PubMed  Google Scholar 

  22. Brock, R., Hamelers, I.H. & Jovin, T.M. Comparison of fixation protocols for adherent cultured cells applied to a GFP fusion protein of the epidermal growth factor receptor. Cytometry 35, 353–362 (1999).

    Article  CAS  Google Scholar 

  23. Pollice, A.A. et al. Sequential paraformaldehyde and methanol fixation for simultaneous flow cytometric analysis of DNA, cell surface proteins, and intracellular proteins. Cytometry 13, 432–444 (1992).

    Article  CAS  Google Scholar 

  24. Hirata, M. & Okamoto, Y. Enumeration of terminal deoxynucleotidyl transferase positive cells in leukemia/lymphoma by flow cytometry. Leuk. Res. 11, 509–518 (1987).

    Article  CAS  Google Scholar 

  25. Melan, M.A. & Sluder, G. Redistribution and differential extraction of soluble proteins in permeabilized cultured cells. Implications for immunofluorescence microscopy. J. Cell Sci. 101, 731–743 (1992).

    PubMed  Google Scholar 

  26. Ohsaki, Y., Maeda, T. & Fujimoto, T. Fixation and permeabilization protocol is critical for the immunolabeling of lipid droplet proteins. Histochem. Cell Biol. 124, 445–452 (2005).

    Article  CAS  Google Scholar 

  27. Nakamura, F. Biochemical, electron microscopic and immunohistological observations of cationic detergent-extracted cells: detection and improved preservation of microextensions and ultramicroextensions. BMC Cell Biol. 2, 10 (2001).

    Article  CAS  Google Scholar 

  28. Burry, R.W. Controls for immunocytochemistry: an update. J. Histochem. Cytochem. 59, 6–12 (2011).

    Article  CAS  Google Scholar 

  29. Mao, S.Y., Javois, L.C. & Kent, U.M. Overview of antibody use in immunocytochemistry. Methods Mol. Biol. 115, 3–10 (1999).

    CAS  PubMed  Google Scholar 

  30. Guillot, P.V., Xie, S.Q., Hollinshead, M. & Pombo, A. Fixation-induced redistribution of hyperphosphorylated RNA polymerase II in the nucleus of human cells. Exp. Cell Res. 295, 460–468 (2004).

    Article  CAS  Google Scholar 

  31. Shibata, T., Tanaka, T., Shimizu, K., Hayakawa, S. & Kuroda, K. Immunofluorescence imaging of the influenza virus M1 protein is dependent on the fixation method. J. Virol. Methods 156, 162–165 (2009).

    Article  CAS  Google Scholar 

  32. Kanda, T., Sullivan, K.F. & Wahl, G.M. Histone-GFP fusion protein enables sensitive analysis of chromosome dynamics in living mammalian cells. Curr. Biol. 8, 377–385 (1998).

    Article  CAS  Google Scholar 

  33. Nasi, S., Cirillo, D., Naldini, L., Marchisio, P.C. & Calissano, P. Microtubules and microfilaments in fixed and permeabilized cells are selectively decorated by nerve growth factor. Proc. Natl. Acad. Sci. USA 79, 820–824 (1982).

    Article  CAS  Google Scholar 

  34. Vielkind, U. & Swierenga, S.H. A simple fixation procedure for immunofluorescent detection of different cytoskeletal components within the same cell. Histochemistry 91, 81–88 (1989).

    Article  CAS  Google Scholar 

  35. Smith-Clerc, J. & Hinz, B. Immunofluorescence detection of the cytoskeleton and extracellular matrix in tissue and cultured cells. Methods Mol. Biol. 611, 43–57 (2010).

    Article  Google Scholar 

  36. Osborn, M., Fanke, W.W. & Weber, K. Visualization of a system of filaments 7–10 nm thick in cultured cells of an epithelioid line (Pt K2) by immunofluorescence microscopy. Proc. Natl. Acad. Sci. USA 74, 2490–2494 (1977).

    Article  CAS  Google Scholar 

  37. Tanaka, K.A. et al. Membrane molecules mobile even after chemical fixation. Nat. Methods 7, 865–866 (2010).

    Article  CAS  Google Scholar 

  38. Giepmans, B.N. Bridging fluorescence microscopy and electron microscopy. Histochem. Cell Biol. 130, 211–217 (2008).

    Article  CAS  Google Scholar 

  39. Leong, A.S. Pitfalls in diagnostic immunohistology. Adv. Anat. Pathol. 11, 86–93 (2004).

    Article  Google Scholar 

  40. Maurisse, R. et al. Comparative transfection of DNA into primary and transformed mammalian cells from different lineages. BMC Biotechnol. 10, 9 (2010).

    Article  Google Scholar 

  41. Simpson, J.C., Wellenreuther, R., Poustka, A., Pepperkok, R. & Wiemann, S. Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. EMBO Rep. 1, 287–292 (2000).

    Article  CAS  Google Scholar 

  42. Pepperkok, R., Simpson, J.C. & Wiemann, S. Being in the right location at the right time. Genome Biol. 2, 1024.1–1024.4 (2001).

    Article  Google Scholar 

  43. Rothbauer, U. et al. Targeting and tracing antigens in live cells with fluorescent nanobodies. Nat. Methods 3, 887–889 (2006).

    Article  CAS  Google Scholar 

  44. Hageman, J., Vos, M.J., van Waarde, M.A. & Kampinga, H.H. Comparison of intra-organellar chaperone capacity for dealing with stress-induced protein unfolding. J. Biol. Chem. 282, 34334–34345 (2007).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank H. van der Want and D. Hoekstra for critically reading the manuscript, A. Algra and R. Hoffmann for technical assistance, O. Sibon for H2B cDNA, H. Kampinga for expression constructs44 used in Figure 2c (University Medical Center Groningen) and V. Cirulli (University of Washington) for EpCAM cDNA. Part of this work was supported by the Groningen University Graduate School of Medical Sciences; a Marie Curie International Reintegration Grant within the 7th European Community Framework Program to B.N.G.G. and was performed at the University Medical Center Groningen Microscopy and Imaging Center, which is sponsored by Netherlands Organization for Scientific Research grants 40-00506-98-9021 and 175-010-2009-023.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ben N G Giepmans.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Text and Figures

Supplementary Figures 1–9 and Supplementary Methods (PDF 3649 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schnell, U., Dijk, F., Sjollema, K. et al. Immunolabeling artifacts and the need for live-cell imaging. Nat Methods 9, 152–158 (2012). https://doi.org/10.1038/nmeth.1855

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nmeth.1855

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