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.

  • Letter
  • Published:

Multi-resolution 3D visualization of the early stages of cellular uptake of peptide-coated nanoparticles

Abstract

A detailed understanding of the cellular uptake process is essential to the development of cellular delivery strategies1 and to the study of viral trafficking2. However, visualization of the entire process, encompassing the fast dynamics (local to the freely diffusing nanoparticle) as well the state of the larger-scale cellular environment, remains challenging3. Here, we introduce a three-dimensional multi-resolution method to capture, in real time, the transient events leading to cellular binding and uptake of peptide (HIV1-Tat)-modified nanoparticles. Applying this new method to observe the landing of nanoparticles on the cellular contour in three dimensions revealed long-range deceleration of the delivery particle, possibly due to interactions with cellular receptors. Furthermore, by using the nanoparticle as a nanoscale ‘dynamics pen’, we discovered an unexpected correlation between small membrane terrain structures and local nanoparticle dynamics. This approach could help to reveal the hidden mechanistic steps in a variety of multiscale processes.

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: Three-dimensional multi-resolution microscopy of the early stages of cellular uptake.
Figure 2: Transient interactions of Tat-coated nanoparticles with the cell surface.
Figure 3: Cell surface terrain features display ‘hot’ dynamics.
Figure 4: Anisotropic diffusion along filopodia.

Similar content being viewed by others

References

  1. Petros, R. A. & DeSimone, J. M. Strategies in the design of nanoparticles for therapeutic applications. Nature Rev. Drug Discov. 9, 615–627 (2010).

    Article  CAS  Google Scholar 

  2. Flint, S. J., Enquist, L. W., Racaniello, V. R. & Skalka, A. M. Principles of Virology Vol. 1 (American Society for Microbiology, 2009).

    Google Scholar 

  3. Sun, E., He, J. & Zhuang, X. Live cell imaging of viral entry. Curr. Opin. Virol. 3, 34–43 (2013).

    Article  CAS  Google Scholar 

  4. Zauner, W., Farrow, N. A. & Haines, A. M. R. In vitro uptake of polystyrene microspheres: effect of particle size, cell line and cell density. J. Control. Rel. 71, 39–51 (2001).

    Article  CAS  Google Scholar 

  5. Geng, Y. et al. Shape effects of filaments versus spherical particles in flow and drug delivery. Nature Nanotech. 2, 249–255 (2007).

    Article  CAS  Google Scholar 

  6. Doherty, G. J. & McMahon, H. T. Mechanisms of endocytosis. Annu. Rev. Biochem. 78, 857–902 (2009).

    Article  CAS  Google Scholar 

  7. Katayama, Y. et al. Real-time nanomicroscopy via three-dimensional single-particle tracking. ChemPhysChem 10, 2458–2464 (2009).

    Article  CAS  Google Scholar 

  8. Ruthardt, N., Lamb, D. C. & Brauchle, C. Single-particle tracking as a quantitative microscopy-based approach to unravel cell entry mechanisms of viruses and pharmaceutical nanoparticles. Mol. Ther. 19, 1199–1211 (2011).

    Article  CAS  Google Scholar 

  9. Müller, B. & Heilemann, M. Shedding new light on viruses: super-resolution microscopy for studying human immunodeficiency virus. Trends Microbiol. 21, 522–533 (2013).

    Article  Google Scholar 

  10. Liu, B. R., Huang, Y-w., Winiarz, J. G., Chiang, H-J. & Lee, H-J. Intracellular delivery of quantum dots mediated by a histidine- and arginine-rich HR9 cell-penetrating peptide through the direct membrane translocation mechanism. Biomaterials 32, 3520–3537 (2011).

    Article  CAS  Google Scholar 

  11. Pelkmans, L., Kartenbeck, J. & Helenius, A. Caveolar endocytosis of simian virus 40 reveals a new two-step vesicular-transport pathway to the ER. Nature Cell Biol. 3, 473–483 (2001).

    Article  CAS  Google Scholar 

  12. Eiriksdottir, E., Mager, I., Lehto, T., El Andaloussi, S. & Langel, U. Cellular internalization kinetics of (luciferin-)cell-penetrating peptide conjugates. Bioconj. Chem. 21, 1662–1672 (2010).

    Article  CAS  Google Scholar 

  13. Barrow, E., Nicola, A. & Liu, J. Multiscale perspectives of virus entry via endocytosis. Virol. J. 10, 177 (2013).

    Article  CAS  Google Scholar 

  14. Vives, E., Brodin, P. & Lebleu, B. A truncated HIV-1 Tat protein basic domain rapidly translocates through the plasma membrane and accumulates in the cell nucleus. J. Biol. Chem. 272, 16010–16017 (1997).

    Article  CAS  Google Scholar 

  15. Lewin, M. et al. Tat peptide-derivatized magnetic nanoparticles allow in vivo tracking and recovery of progenitor cells. Nature Biotechnol. 18, 410–414 (2000).

    Article  CAS  Google Scholar 

  16. Tyagi, M., Rusnati, M., Presta, M. & Giacca, M. Internalization of HIV-1 Tat requires cell surface heparan sulfate proteoglycans. J. Biol. Chem. 276, 3254–3261 (2001).

    Article  CAS  Google Scholar 

  17. Gentile, M. et al. Determination of the size of HIV using adenovirus type 2 as an internal length marker. J. Virol. Methods 48, 43–52 (1994).

    Article  CAS  Google Scholar 

  18. Hewlett, L., Prescott, A. & Watts, C. The coated pit and macropinocytic pathways serve distinct endosome populations. J. Cell Biol. 124, 689–703 (1994).

    Article  CAS  Google Scholar 

  19. Fuchs, S. M. & Raines, R. T. Pathway for polyarginine entry into mammalian cells. Biochemistry 43, 2438–2444 (2004).

    Article  CAS  Google Scholar 

  20. Cang, H., Xu, C. S., Montiel, D. & Yang, H. Guiding a confocal microscope by single fluorescent nanoparticles. Opt. Lett. 32, 2729–2731 (2007).

    Article  Google Scholar 

  21. Cang, H., Wong, C. M., Xu, C. S., Rizvi, A. H. & Yang, H. Confocal three dimensional tracking of a single nanoparticle with concurrent spectroscopic readouts. Appl. Phys. Lett. 88, 223901 (2006).

    Article  Google Scholar 

  22. Cang, H., Montiel, D., Xu, C. S. & Yang, H. Observation of spectral anisotropy of gold nanoparticles. J. Chem. Phys. 129, 044503 (2008).

    Article  Google Scholar 

  23. Montiel, D., Cang, H. & Yang, H. Quantitative characterization of changes in dynamical behavior for single-particle tracking studies. J. Phys. Chem. B 110, 19763–19770 (2006).

    Article  CAS  Google Scholar 

  24. Brenner, H. The slow motion of a sphere through a viscous fluid towards a plane surface. Chem. Eng. Sci. 16, 242–251 (1961).

    Article  CAS  Google Scholar 

  25. Lin, B., Yu, J. & Rice, S. A. Direct measurements of constrained Brownian motion of an isolated sphere between two walls. Phys. Rev. E 62, 3909–3919 (2000).

    Article  CAS  Google Scholar 

  26. Schmidt, N., Mishra, A., Lai, G. H. & Wong, G. C. L. Arginine-rich cell-penetrating peptides. FEBS Lett. 584, 1806–1813 (2010).

    Article  CAS  Google Scholar 

  27. Mattila, P. K. & Lappalainen, P. Filopodia: molecular architecture and cellular functions. Nature Rev. Mol. Cell Biol. 9, 446–454 (2008).

    Article  CAS  Google Scholar 

  28. Lehmann, M. J., Sherer, N. M., Marks, C. B., Pypaert, M. & Mothes, W. Actin- and myosin-driven movement of viruses along filopodia precedes their entry into cells. J. Cell Biol. 170, 317–325 (2005).

    Article  CAS  Google Scholar 

  29. Sherer, N. M. et al. Retroviruses can establish filopodial bridges for efficient cell-to-cell transmission. Nature Cell Biol. 9, 310–315 (2007).

    Article  CAS  Google Scholar 

  30. Aggarwal, A. et al. Mobilization of HIV spread by diaphanous 2 dependent filopodia in infected dendritic cells. PLoS Pathogens 8, e1002762 (2012).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors thank S. McManus for assistance with TEM measurements. This work was supported by the US Department of Energy (DE-SC0006838) and by Princeton University.

Author information

Authors and Affiliations

Authors

Contributions

K.W. and H.Y. conceived and designed the experiments. K.W. performed the experiments. K.W. and H.Y. analysed the data. K.W. and H.Y. wrote the paper.

Corresponding author

Correspondence to Haw Yang.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary information

Supplementary Information (PDF 7744 kb)

Supplementary movie 1

Supplementary movie 1 (MP4 24503 kb)

Supplementary movie 2

Supplementary movie 2 (MP4 7423 kb)

Supplementary movie 3

Supplementary movie 3 (MP4 1702 kb)

Supplementary movie 4

Supplementary movie 4 (MP4 24156 kb)

Supplementary movie 5

Supplementary movie 5 (MP4 3753 kb)

Supplementary movie 6

Supplementary movie 6 (MP4 24136 kb)

Supplementary movie 4

Supplementary movie 4 (MP4 2170 kb)

Supplementary movie 5

Supplementary movie 5 (MP4 881 kb)

Supplementary movie 6

Supplementary movie 6 (MP4 16106 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Welsher, K., Yang, H. Multi-resolution 3D visualization of the early stages of cellular uptake of peptide-coated nanoparticles. Nature Nanotech 9, 198–203 (2014). https://doi.org/10.1038/nnano.2014.12

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nnano.2014.12

This article is cited by

Search

Quick links

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research